Ester compound, active agent for controlling noxious insect pests containing the same as active ingredient, intermediate for production of the ester compound and process for producing the intermediate

ABSTRACT

The present invention provides a compound represented by the formula: ##STR1## wherein R 1  denotes a hydrogen atom or a methyl group; R 2  represents a 1-methyl-2-propenyl group, a 1-methyl-2-propynyl group, a 3,3-dihalogeno-1-methyl-2-propenyl group or a C 1  -C 6  alkyl group which may be substituted with at least one halogen atom; and A&#39; represents a hydrogen atom or a protecting group for a hydroxyl group. The compound is useful in the preparation of esters which can be used to control insect pests.

This is a division of application Ser. No. 08/294,934, filed Aug. 23,1994 now U.S. Pat. No. 5,550,258.

FIELD OF THE INVENTION

The present invention relates to an ester compound, an active agent forcontrolling noxious insect pests containing the ester compound as anactive ingredient, an intermediate for production of the ester compound,and a process for producing the intermediate.

DESCRIPTION OF THE RELATED ART

Certain ester compounds have been disclosed as an active ingredient ofpesticides, for example, in JAPANESE PATENT KOKAIs (Laid Open)No.S-56-75459 and No.S-57-67537. However, these ester compounds are notsatisfactory for controlling noxious insect pests.

SUMMARY OF THE INVENTION

As a result of extensive study, the inventors have found that an estercompound represented by a formula I (shown below) having a uniquealcohol moiety of the formula II is much more effective for controllingnoxious insect pests. They also found useful processes which can providesaid ester compound and said alcohol compound in good yields.

Thus the present invention provides an ester compound (hereinafterreferred to as `the present compound`) represented by a formula I:##STR2## wherein R₁ denotes a hydrogen atom or a methyl group; R₂represents a 1-methyl-2-propenyl group, a 1-methyl-2-propynyl group, a3,3-dihalogeno-1-methyl-2-propenyl group, or a C₁ -C₆ alkyl group whichmay be substituted with at least one halogen atom;

R₃ represents an acid residue of pyrethroids.

It also provides an pesticidal agent containing the same as an activeingredient for controlling noxious insect pests.

The present invention further provides an intermediate alcohol compoundrepresented by the formula II: ##STR3## wherein R₁ and R₂ are the sameas defined above, a process for producing the ester compound I and aprocess for producing the alcohol compound II.

PREFERRED EMBODIMENT OF THE INVENTION

The ester compound of the present invention shows good effect forcontrolling noxious insects, acarines or mites and nematodes.

First, description will be made on the ester compound represented by theformula I: ##STR4## wherein R₁, R₂ and R₃ are the same as defined above.

Preferably 3,3-dihalogeno-1-methyl-2-propenyl group for R₂ is a3,3-difluoro-1-methyl-2-propenyl group or a3,3-dichloro-1-methyl-2-propenyl group.

Preferable C₁ -C₆ alkyl groups which may be substituted with at leastone halogen atom for R₂ include a 2,2,2-trifluoroethyl group, a2,2-difluoroethyl group, a pentafluoroethyl group, a 2-fluoroethylgroup, a 3-fluoropropyl group, a methyl group, an ethyl group, an-propyl group, and an i-propyl group.

When the substituent R₂ of the present compound represents a C₁ -C₆alkyl group which may be substituted with at least one halogen atom,preferable examples of the R₂ are a C₂ -C₄ alkyl group which may besubstituted at least one fluorine atom such as a 2-fluoroethyl group, a2,2,2-trifluoroethyl group or an ethyl group.

When the C₁ -C₆ alkyl group which may be substituted with at least onehalogen atom for R₂ is a methyl group, an ethyl group, n-propyl group, a2-fluoroethyl group, a 2,2,2-trifluoroethyl group or a 3-fluoropropylgroup, R₁ is preferably a methyl group.

When the substituent R₂ of the present compound represents a1-methyl-2-propenyl group, a 1-methyl-2-propynyl group, a3,3-dihalogeno-1-methyl-2-propenyl group or an isopropyl group, R₁ ispreferably a hydrogen atom.

The acid residue of pyrethroids represented by R₃ (acid residue heremeans the group other than a carboxyl group of a carboxylic acid) may beany residue which can provide an active pyrethroid ester.

However, preferably R₃ is represented by a formula III: ##STR5## whereinZ₁ denotes a hydrogen atom or a methyl group; and

Z₂ represents a hydrogen atom, a C₁ -C₆ alkyl group, a C₁ -C₆ alkoxygroup, a (C₁ -C₆ alkoxy)methyl group, a (C₁ -C₆ alkoxy)ethyl group, a C₂-C₄ alkenyloxy group, a C₂ -C₄ alkynyloxy group, a (C₂ -C₄alkenyl)oxymethyl group, or a (C₂ -C₄ alkynyl)oxymethyl group, all ofwhich except the hydrogen atom may be substituted with at least onehalogen atom,

Z₂ may alternatively represent a group of a formula IV: ##STR6## whereinZ₃ denotes a hydrogen atom or a halogen atom; T₁ and T₂ may be the sameor different, each denotes a hydrogen atom, a halogen atom, a cyanogroup, or a C₁ -C₃ alkyl group or a phenyl group, the last two of whichmay be substituted with at least one halogen atom;

T₁ and T₂ may be combined with each other at their terminals to form aC₃ -C₆ cycloalkyl group or a group represented by a formula V: ##STR7##wherein B denotes an oxygen atom or a sulfur atom, or Z₂ canalternatively represent a group of a formula VI: ##STR8## wherein Drepresents a hydrogen atom or a halogen atom; and G denotes a C₁ -C₆alkyl group, a C₃ -C₅ cycloalkyl group or a phenyl group, all of whichmay be substituted with at least one halogen atom.

Alternatively R₃ may be a group represented by a formula VII: ##STR9##wherein J denotes a halogen atom or a C₁ -C₆ alkyl group or a C₁ -C₆alkoxy group, the last two of which may be substituted with at least onehalogen atom.

Preferable Z₂ group for the formula III includes a methyl group, anethoxy group, a n-propoxy group, a n-butoxy group, an allyloxy group, apropargyloxy group, an allyoxymethyl group, a propargyloxymethyl groupand a 2,2,2-trifluoroethoxy.

When Z₂ group represents the formula III, Z₃ is preferably a hydrogenatom; and T₁ and T₂ are same or different and each represents a methylgroup, a chlorine atom, a bromine atom, a trifluoromethyl group, afluorine atom, a p-chlorophenyl group or a cyano group.

When Z₂ group represents the formula VI, D represents preferably ahydrogen atom or a fluorine atom and G is preferably a 2-fluoroethylgroup, a 1,1,1,3,3,3-hexafluoropropan-2-yl group, a 2,2,2-trifluoroethylgroup, a methyl group or an ethyl group.

When R₃ represents the formula VII, preferably the substituent J is afluorine atom, a chlorine atom, a trifluoromethyl group, adifluoromethyl group, trifluoromethoxy group or a difluoromethoxy group.

The halogen atom contained in the present compound includes a fluorineatom, a chlorine atom and a bromine atom.

The present compound can be produced by one of the following methods.

Method A:

A method of producing the present compound of the formula I whichcomprises reacting an alcohol compound represented by a formula II:##STR10## wherein R₁ and R₂ represent those specified above, with acarboxylic acid represented by a formula VIII:

    R.sub.3 --COOH                                             VIII

wherein R₃ denotes those specified above or a reactive derivativethereof.

Typical examples of the reactive derivative of the carboxylic acidinclude an acid halide and an acid anhydride.

The reaction can be conducted in an inert solvent in the presence of anappropriate condensing agent or base. The condensing agent to be usedmay be dicyclohexylcarbodiimide (DCC) or1-ethyl-3-(3-diemthylaminopropyl)carbodiimide hydrochloride (WSC).

The base to be used may be an organic base such as triethylamine,pyridine, 4-dimethylaminopyridine, or diisopropylethylamine.

Typical examples of the inert solvent include hydrocarbons like benzene,toluene, and hexane; ethers like diethyl ether and tetrahydrofuran; andhalogenated hydrocarbons such as dichloromethane and 1,2-dichloroethane.

A possible reaction temperature range is between -20° C. and 100° C. orthe boiling point of the solvent used for the reaction; or morepreferably between -5° C. and 100° C. or the boiling point of thesolvent. The molar ratio of the alcohol compound represented by theformula II to the carboxylic acid represented by the formula XI or thereactive derivative thereof may be determined optionally, but isapproximately one, preferably one. An equivalent to excess moles, ormore specifically one to five moles, of the condensing agent or the basemay be used according to the requirements to one mole of the alcoholcompound represented by the formula II.

After completion of the reaction, the reaction solution is subjected toa conventional post-treatment such as solvent extraction and/orconcentration to yield the present compound. The present compoundobtained may be purified by column chromatography, distillation orrecrystallization.

Method B:

A method of producing the present compound I which comprises reacting anester derivative represented by a formula IX: ##STR11## wherein R₁, R₂,and R₃ represent those specified above, in the presence of a base with aphosphonium salt represented by a formula X: ##STR12## wherein X denotesa halogen atom such as a chlorine atom, a bromine atom or an iodineatom.

The reaction is usually conducted in an organic solvent, which may be anether like diethyl ether, dimethoxyethane, or tetrahydrofuran or ahydrocarbon like hexane or toluene. A mixture of two or more organicsolvents may be used.

Typical examples of the base to be used in the reaction includealkyllithiums such as n-butyllithium and methyllithium, and alkalinemetal alkoxides (e.g. C₁ -C₄ alkoxides such as potassium t-butoxide andsodium methoxide). A commercially available phosphonium salt (forexample, methyltriphenyl phosphonium bromide by Aldrich Corp.) may beused as it is or purified if necessary.

The reaction temperature range is usually between -78° C. and 100° C. orthe boiling point of the solvent used for the reaction, preferablybetween -78° C. and 30° C. One or two moles of the phosphonium saltrepresented by the formula X and one or two moles of the base are usedto one mole of the ester derivative of the formula IX.

After completion of the reaction, the reaction solution is subjected toa conventional post-treatment such as solvent extraction and/orconcentration to yield the present compound. The present compoundobtained may be purified by column chromatography, distillation orrecrystallization.

Method C:

A process for producing the present compound of the formula I whichcomprises reacting the ester derivative represented by the formula IXwith a reaction mixture of (a) zinc (b) dibromomethane or diiodomethaneand (c) titanium tetrachloride in an inert organic solvent.

The reaction is usually conducted in an inert organic solvent, which maybe a halogenated hydrocarbon like dichloromethane or 1,2-dichloroethane,an ether like tetrahydrofuran, or a hydrocarbon like hexane or toluene.Two or more organic solvents may be mixed at an optional ratio ifnecessary.

A commercially available titanium tetrachloride (for example, thespecial grade by Kanto Chemical Corp.) may be used as it is or dilutedwith an organic solvent such as dichloromethane or toluene.

Usually 0.5 to 5 moles, preferably 0.9 to 1.2 moles of titaniumtetrachloride is used to one mole of the ester derivative represented bythe formula IX.

Zinc powder (zinc dust) is usually used for the reaction. Commerciallyavailable zinc dust (for example, zinc dust of approximately 325 mesh byAldrich Corp.) may be used as it is or further activated according to amethod specified in `Reagents for Organic Synthesis`, (Fieser et al.,Vol. 1, p1276 (1967)).

Usually 2 to 50 moles, preferably 4 to 10 moles of zinc is used to onemole of the ester derivative of the formula IX.

The amount of dibromomethane or diiodomethane to be used to one mole oftitanium tetrachloride is usually 1 to 10 moles, preferably 1 to 5moles.

Titanium tetrachloride is usually added dropwise to a mixture ofdibromomethane or diiodomethane and zinc in an inert organic solvent ata temperature of -40° C. to 50° C., preferably -20° C. to 5° C. Afterthe reaction mixture is stirred at a temperature in these ranges, range,the ester derivative represented by the formula IX is added to theresultant reaction mixture and the mixture is usually further stirred atthe temperature.

After completion of the reaction, sodium hydrogencarbonate and water areadded to the reaction solution, and then filtered, the filtrate maysubjected to a post-treatment such as solvent extraction orconcentration to isolate the present compound. The reaction solutioncontaining the compound may be used for a subsequent reaction process.The compound isolated may be purified by column chromatography ordistillation if necessary.

The compound may have stereoisomers (R,S) or geometrical isomers (E,Z).The invention includes all the stereoisomers, geometrical isomers, andmixtures thereof having activities for controlling noxious organisms.

In the above methods A, B and C optically active compounds of thepresent invention may be obtained from optically active startingmaterials without causing racemization.

Next, description will be made on the intermediate alcohol compounds ofthe formula II used in the method A above. Typical examples of thealcohol compound include:

(RS)-3-ethyl-2-methyl-4-methylidene-2-cyclopentenol;

(1RS)-3-(1-methyl-2-propynyl)-4-methylidene-2-cyclopentenol;

(1RS)-3-(1-methyl-2-propenyl)-4-methylidene-2-cyclopentenol;

(1RS)-3-(1-methyl-(3,3-dichloro-2-propenyl))-4-methylidene-2-cyclopentenol;

(RS)-3-isopropyl-4-methylidene-2-cyclopentenol;

(RS)-3-(2,2,2-trifluoroethyl)-2-methyl-4-methylidene-2-cyclopentenol;

(RS)-3-(2-fluoroethyl)-2-methyl-4-methylidene-2-cyclopentenol;

(RS)-3-(3-fluoropropyl)-2-methyl-4-methylidene-2-cyclopentenol;

(S)-3-ethyl-2-methyl-4-methylidene-2-cyclopentenol;

(1S)-3-(1-methyl-2-propynyl)-4-methylidene-2-cyclopentenol;

(1S)-3-(1-methyl-2-propenyl)-4-methylidene-2-cyclopentenol;

(1RS)-3-(2,2,2-trifluoroethyl)-2-methyl-4-methylidene-2-cyclopentenol;

(S)-3-(2-fluoroethyl)-2-methyl-4-methylidene-2-cyclopentenol; and

(S)-3-(3-fluoropropyl)-2-methyl-4-methylidene-2-cyclopentenol.

The alcohol compound of the formula II may be produced according to amethod shown by a scheme I below: ##STR13## wherein R₁ and R₂ representthose specified above and A represents a protecting group for a hydroxylgroup.

The protecting group A for a hydroxyl group may be any that does notadversely affect the reaction. Preferable examples of the protectinggroup A include: tri(C₁ -C₆)alkylsilyl groups such as a trimethylsilylgroup, a triethylsilyl group and a t-butyldimethylsilyl group;2-tetrahydrofuranyl group; 2-tetrahydropyranyl group; and a (C₁-C₂)alkyl group substituted with a (C₁ -C₂)alkoxy group at theα-position such as a methoxymethyl group, a 1-methoxyethyl group, anethoxymethyl group or a 1-ethoxyethyl group.

Examples of the alcohol derivative represented by the formula XIinclude:

(RS)-2-methyl-4-methylidene-3-ethyl-1-trimethylsilyloxy-2-cyclopentene;

(1RS)-4-methylidene-3-(1-methyl-2-propynyl)-1-trimethylsilyloxy-2-cyclopentene;

(1RS)-4-methylidene-3-(1-methyl-2-propenyl)-1-t-butyldimethylsilyloxy-2-cyclopentene;

(RS)-4-methylidene-3-isopropyl-1-triethylsilyloxy-2-cyclopentene;

(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)-1-triisopropylsilyloxy-2-cyclopentene;

(RS)-2-methyl-4-methylidene-3-(2-fluoroethyl)-1-t-butyldimethylsilyloxy-2-cyclopentene;

(RS)-2-methyl-4-methylidene-3-(3-fluoropropyl)-1-triethylsilyloxy-2-cyclopentene;

(RS)-2-methyl-4-methylidene-3-ethyl-1-methoxymethyloxy-2-cyclopentene;

(S)-4-methylidene-3-(1-methyl-2-propynyl)-1-(2-tetrahydropyranyl)oxy-2-cyclopentene;and

(RS)-4-methylidene-3-(1-methyl-2-propenyl)-1-ethoxyethyloxy-2-cyclopentene.

In the scheme I, the compound of the formula XIII can be produced, forexample, by a method disclosed in JAPANESE PATENT KOKAI (Laid Open)No.S-57-67537.

The process D for directly producing the alcohol compound represented bythe formula II from the compound of the formula XIII is conducted by themethod B described above.

Namely, the alcohol compound of the formula II produced by using thecompound XIII as a starting material in place of the ester derivative ofthe formula IX.

The process E for protecting a hydroxyl group of the cyclopentenolonecompound XIII to produce the compound XII is conducted according to amethod specified in `Protective Group in Organic Synthesis` (T. W.Greene and P. G. M. Wuts; 2nd edition, John Wiley & Sons, Inc. pages10-86, (1991)).

However, preferably the process is conducted by one of the followingmethods (i) to (iii).

(i) When A represents tri(C₁ -C₆)alkylsilyl group;

The protecting of the hydroxy group of the cyclopentenolone compoundXIII is carried out by reacting a tri(C₁ -C₆)alkylsilyl chloride ortri(C₁ -C₆)alkylsilyl triflate with the cyclopentenolone compound XIIIin the presence of a base.

The reaction is usually conducted in an inert organic solvent. Examplesof the solvent are a halogenated hydrocarbon solvent likedichloromethane, an ether solvent like tetrahydrofuran or diethyl etheror a polar aprotic solvent like N,N-dimethylformamide.

1 to 10 moles, preferably 1.2 to 5 moles of an organic base likeimidazole, triethylamine, diisopropylethylamine, pyridine or2,6-dimethylpyridine and 1 to 2 moles, preferably 1 to 1.5 moles oftri(C₁ -C₆)alkylsilyl chloride or tri(C₁ -C₆)alkylsilyl triflate areused to 1 mole of the cyclopentenolone compound.

The reaction temperatures is usually -30° C. to 50° C., preferably -10°C. to 30° C.

ii) When A represents 2-tetrahydrofuranyl group or 2-tetrahydropyranylgroup;

The protecting of the hydroxy group of the cyclopentenolone compoundXIII is carried out by reacting dihydropyran or dihydrofuran with thecyclopentenolone compound XIII in the presence of an acid.

The reaction may be conducted in an aprotic organic solvent such as anether solvent like diethyl ether or tetrahydrofuran, a hydrocarbonsolvent like benzene or toluene, or a halogenated hydrocarbon solventlike dichloromethane or chloroform.

1 to 50 moles, preferably 1 to 10 moles of dihydropyran or dihydrofuranare allowed to react with the compound XIII in the presence of acatalytic amount of an acid such as organic acid (e.g. p-toluenesulfonicacid or pyridine p-toluenesulfonate) or an inorganic acid, such asphosphoric acid, hydrochloric acid, or sulfuric acid at 0° C. to 30° C.or at an ambient temperature.

(iii) When A represents a (C₁ -C₂)alkyl group substituted with a (C₁-C₂)alkoxy group at the α-position;

The protecting of the hydroxy group of the cyclopentenolone compound iscarried out by reacting a (C₁ -C₂)alkyl chloride group substituted witha (C₁ -C₂)alkoxy group at the α-position with the cyclopentenolonecompound XIII in the presence of a base.

Examples of the solvent to be used are a halogenated hydrocarbon solventlike dichloromethane or chloroform, an ether solvent like diethyl etheror tetrahydrofuran, or a hydrocarbon solvent like benzene or toluene.

1 to 10 moles, preferably 1 to 5 moles of an organic base liketriethylamine, diisopropylethylamine, or 2,6-diemthylpyridine or analkaline metal hydride like sodium hydride or potassium hydride and 1 to50 moles, preferably 1 to 5 moles of a (C₁ -C₂)alkyl chloridesubstituted with a (C₁ -C₂)alkoxy group at the α-position are allowed toreact with the compound at a temperature of -20° C. to 50° C.,preferably 0° C. to 20° C.

The process F for preparing the compound IX from the compound XII isconducted according to the method C described above using the compoundXII as a starting material in place of the ester derivative of theformula IX.

The compound XI may be produced according to the method B describedabove using the compound XII as a starting material in place of theester derivative of the formula IX.

The process G for producing the alcohol compound of the formula II fromthe compound XI is conducted according to a method specified in`Protective Group in Organic Synthesis` (T. W. Greene and P. G. M. Wuts;2nd edition, John Wiley & Sons, Inc. pp10-86, (1991)).

However, preferably the process is carried out by one of the followingmethods (i) to (iii).

(i) When A represents tri(C₁ -C₆)alkylsilyl group;

The removing of the protecting group is carried out by contacting thealcohol derivative of the formula III with an acid or a fluoride anion.

Examples of an acid are: an ether solvent like tetrahydrofuran ordiethyl ether, a halogenated hydrocarbon solvent like dichloromethane, ahydrocarbon solvent like benzene or toluene, or a protic solvent likewater, methanol, or ethanol, an inorganic acid like hydrochloric acid,or sulfuric acid, or an organic acid such as formic acid or acetic acid,which may be mixed with water if necessary.

Examples of a fluoride anion are tetrabutylammonium fluoride andhydrofluoric acid.

The reaction temperature is usually 0° C. to 30° C.

(ii) When A represents 2-tetrahydrofuranyl group or 2-tetrahydropyranylgroup;

The removing of the protecting group is carried out by contacting thealcohol derivative of the formula III with a catalytic to excess amountof an acid (an organic acid like p-toluenesulfonic acid or a saltthereof, or an inorganic acid like hydrochloric acid or sulfuric acid).

The reaction is usually conducted in a protic solvent, such as water,methanol, or ethanol, or a mixed solvent of the protic solvent and anether solvent, such as diethyl ether or tetrahydrofuran.

The reaction temperature is usually 0° C. to 50° C.

(iii) When A represents a (C₁ -C₂)alkyl group substituted with a (C₁-C₂)alkoxy group at the α-position;

The removing of the protecting group is carried out by contacting thealcohol derivative XI with a catalytic to excess amount of an acid suchas an organic acid like formic acid, acetic acid, or methanesulfonicacid or an inorganic acid like hydrochloric acid or sulfuric acid.

The reaction is usually conducted in a protic solvent, such as water,methanol or ethanol, or a mixed solvent of the protic solvent and anether solvent such as diethyl ether or tetrahydrofuran.

The reaction temperature is usually 20° C. to the refluxing temperatureof the solvent.

In the above method (i), (ii) or (iii) the alcohol derivative XIobtained in a solution form by usual post-treatment after theolefination process can be used as it is without isolating.

The ester derivative of the formula IX used as a starting material inthe method B and the method C may be prepared, for example, according toa method disclosed in JAPANESE PATENT KOKAI (Laid Open No.S-56-75459 andNo. S-57-67537.

Preferable examples of the present ester compounds are shown in theTable 1 below.

                                      TABLE 1                                     __________________________________________________________________________                                                    Notation of                                                                            Physical                                Notation of                  stereoisomerism                                                                        constant             Com-               stereoisomerism              of the   (Refractive          pound              of the alcohol               carboxylic                                                                             Index)               No.  R.sub.1                                                                          R.sub.2    moiety  R.sub.3              acid moiety                                                                            n.sub.D                                                                       (°C.)         __________________________________________________________________________    1    CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR14##           (1R)-trans                                                                             1.5070 (20.5)        2    H                                                                                 ##STR15## (RS)                                                                                   ##STR16##           (1R)-cis, trans                                                                        1.5076 (23)          3    H                                                                                 ##STR17## (RS)                                                                                   ##STR18##           (1R)-trans                    4    H                                                                                 ##STR19## (RS)                                                                                   ##STR20##           (1R)-trans                                                                             1.5251 (24.5)        5    CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR21##           (1R)-trans                                                                             1.5251 (23)          6    H                                                                                 ##STR22## (RS)                                                                                   ##STR23##           (1RS)-cis (Z)                                                                          1.4804 (26)          7    H                                                                                 ##STR24## (RS)                                                                                   ##STR25##           (1RS)-cis, trans              8    H                                                                                 ##STR26## (RS)                                                                                   ##STR27##           (1R)-trans                                                                             1.5902 (25)          9    CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR28##           --       1.4991 (23.5)        10   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR29##           (1RS)-trans                                                                            1.4848 (25)          11   H                                                                                 ##STR30## (RS)                                                                                   ##STR31##           (1R)-trans                                                                             1.5197 (25)          12   H                                                                                 ##STR32## (RS)                                                                                   ##STR33##           --       1.5023 (23)          13   H                                                                                 ##STR34## (RS)                                                                                   ##STR35##           (1R)-trans                    14   CH.sub.3                                                                         CH.sub.3   (RS)                                                                                   ##STR36##           (1RS)-trans                                                                            1.4883 (25)          15   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR37##           (1R)-trans                                                                             1.4805 (21)          16   H                                                                                 ##STR38## (RS)                                                                                   ##STR39##           (S)                           17   H                                                                                 ##STR40## (RS)                                                                                   ##STR41##           (1R)-trans (EZ)                                                                        1.5014 (23.5)        18   H                                                                                 ##STR42## (RS)                                                                                   ##STR43##           (1R)-trans                    19   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR44##           (1R)-trans                                                                             1.5061 (24)          20   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR45##           (1R)-cis 1.5102 (22.5)        21   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR46##           (1R)-cis, trans                                                                        1.5070 (23.5)        22   H                                                                                 ##STR47## (RS)                                                                                   ##STR48##           (1RS)- trans                                                                           1.4797 (25)          23   H                                                                                 ##STR49## (RS)                                                                                   ##STR50##           (1R)-trans                    24   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR51##           (1R)-trans                                                                             1.4930 (23.5)        25   H                                                                                 ##STR52## (RS)                                                                                   ##STR53##           (1R)-cis (E)                  26   H                                                                                 ##STR54## (RS)                                                                                   ##STR55##           (1R)-trans                    27   H                                                                                 ##STR56## (RS)                                                                                   ##STR57##           --       1.4917 (26.5)        28   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR58##           (1R)-cis (E)                  29   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR59##           (1R)-trans (E/Z)                                                                       1.5045 (25)          30   CH.sub.3                                                                         n-C.sub.3 H.sub.7                                                                        (RS)                                                                                   ##STR60##           (1R)-trans                    31   H                                                                                 ##STR61## (RS)                                                                                   ##STR62##           (1R)-cis (E)                  32   H                                                                                 ##STR63## (RS)                                                                                   ##STR64##           (1R)-cis, trans                                                                        1.4995 (27.0)        33   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR65##           (1RS)-trans                   34   H                                                                                 ##STR66## (RS)                                                                                   ##STR67##           (1R)- trans (E/Z)                                                                      1.5047 (24.5)        35   H                                                                                 ##STR68## (RS)                                                                                   ##STR69##           (1RS)-cis, trans              36   H                                                                                 ##STR70## (RS)                                                                                   ##STR71##           (1R)-trans                    37   CH.sub.3                                                                         CH.sub.3   (RS)                                                                                   ##STR72##           (1R)-cis, trans                                                                        1.5098 (22)          38   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR73##           (1R)                          39   H                                                                                 ##STR74## (RS)                                                                                   ##STR75##           (1R)-cis (E)                  40   H                                                                                 ##STR76## (RS)                                                                                   ##STR77##           (1R)-cis (E)                  41   H                                                                                 ##STR78## (RS)                                                                                   ##STR79##           (1R)-trans (Z)                42   H                                                                                 ##STR80## (RS)                                                                                   ##STR81##           (1R)-cis (E)                  43   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR82##           --       1.4687 (24)          44   CH.sub.3                                                                         CH.sub.3   (RS)                                                                                   ##STR83##           --       1.4980 (22)          45   CH.sub.3                                                                         C.sub.2 H.sub.5                                                                          (RS)                                                                                   ##STR84##           (1RS)-cis (E)                                                                          1.4969 (23.5)        46   H                                                                                 ##STR85## (RS)                                                                                   ##STR86##           (1R)- trans                   47   H                                                                                 ##STR87## (RS)                                                                                   ##STR88##           --                            48   H                                                                                 ##STR89## (RS)                                                                                   ##STR90##           (1RS)-cis (Z)                 49   H                                                                                 ##STR91## (RS)                                                                                   ##STR92##           (1R)- trans                   50   CH.sub.3                                                                         FCH.sub.2 CH.sub.2 CH.sub.2                                                              (RS)                                                                                   ##STR93##           (1R)-trans                    51   CH.sub.3                                                                         FCH.sub.2 CH.sub.2                                                                       (RS)                                                                                   ##STR94##           (1R)-trans                    52   CH.sub.3                                                                         FCH.sub.2 CH.sub.2 CH.sub.2                                                              (RS)                                                                                   ##STR95##           --                            53   CH.sub.3                                                                         FCH.sub.2 CH.sub.2                                                                       (RS)                                                                                   ##STR96##           --                            54   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR97##           (1R)-trans                                                                             1.4999 (21)          55   H                                                                                 ##STR98## (RS)                                                                                   ##STR99##           (1R)- trans                   56   H                                                                                 ##STR100##                                                                              (RS)                                                                                   ##STR101##          (1R)-trans (E/Z)              57   H                                                                                 ##STR102##                                                                              (RS)                                                                                   ##STR103##          (1R)-trans                    58   H                                                                                 ##STR104##                                                                              (RS)                                                                                   ##STR105##          (1R)- trans                   59   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR106##          (1R)-trans                    60   CH.sub.3                                                                         CH.sub.3 CH.sub.2 CH.sub.2                                                               (RS)                                                                                   ##STR107##          (1R)-trans                    61   CH.sub.3                                                                         CH.sub.3 CH.sub.2 CH.sub.2                                                               (RS)                                                                                   ##STR108##          --                            62   H                                                                                 ##STR109##                                                                              (RS)                                                                                   ##STR110##          (1R)-trans                    63   H                                                                                 ##STR111##                                                                              (RS)                                                                                   ##STR112##          (1R)-cis                      64   H                                                                                 ##STR113##                                                                              (RS)                                                                                   ##STR114##          (1R)-trans (E/Z)              65   H                                                                                 ##STR115##                                                                              (RS)                                                                                   ##STR116##          (1R)-cis (Z)                  66   H                                                                                 ##STR117##                                                                              (RS)                                                                                   ##STR118##          (1R)-trans                    67   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR119##          (1R)-cis (E)                  68   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR120##          (1R)-trans (E)                69   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR121##          (1R)-trans (E)                70   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR122##          (1R)-trans (E)                                                                         1.4940 (22)          71   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR123##          (1R)-cis                      72   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR124##          (S)      1.4879 (23)          73   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR125##          (S)                           74   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR126##          (1R)-cis (Z)                  75   CH.sub.3                                                                         F.sub.2 CHCH.sub.2                                                                       (RS)                                                                                   ##STR127##                                        76   CH.sub.3                                                                         FCH.sub.2 CH.sub.2                                                                       (RS)                                                                                   ##STR128##                                        77   CH.sub.3                                                                         CF.sub.3 CF.sub.2                                                                        (RS)                                                                                   ##STR129##          (1R)-trans                    78   CH.sub.3                                                                         FCH.sub.2 CH.sub.2                                                                       (RS)                                                                                   ##STR130##          (1R)-trans                    79   CH.sub.3                                                                         F.sub.2 CHCH.sub.2                                                                       (RS)                                                                                   ##STR131##          (1R)-trans                    80   CH.sub.3                                                                         FCH.sub.2 CH.sub.2 CH.sub.2                                                              (RS)                                                                                   ##STR132##          (1R)-trans                    81   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR133##          (IR)-cis (E)                  82   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR134##          (1R)-trans                    83   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR135##          (1RS)-trans                   84   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR136##          (1RS)-cis (Z)                 85   CH.sub.3                                                                         CF.sub.3 CF.sub.2                                                                        (RS)                                                                                   ##STR137##          (1R)-cis (Z)                  86   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR138##          (1R)-trans                    87   CH.sub.3                                                                         CF.sub.3 CH.sub.2                                                                        (RS)                                                                                   ##STR139##          (1R)-trans (E/Z)              88   CH.sub.3                                                                         FCH.sub.2 CH.sub.2                                                                       (RS)                                                                                   ##STR140##          (1R)-trans (E/Z)              89   CH.sub.3                                                                         CF.sub.3 CF.sub.2                                                                        (RS)                                                                                   ##STR141##          (1R)-trans                    90   CH.sub.3                                                                         F.sub.2 CHCH.sub.2                                                                       (RS)                                                                                   ##STR142##          (1R)-trans                    __________________________________________________________________________

The compound of the present invention is effective for controllingnoxious insects, mites and nematodes listed below:

Hemiptera:

Delphacidae (leaf hoppers) such as Laodelphax striatellus, Nilparvatelugens and Sogatella furcifera; Cicadelloidea (leaf hoppers) such asNephotettix cincticeps and Nephotettix virescens, Aphididea (aphids),Pentatomidae (stink bugs), Aleyrodidae, Coccoidea (scale insects),Tingidae (lacebugs), Psyllidae (jumping plant-lices), etc.;

Lepidoptera:

Pyralidae such as Chilo suppressalis and Cnaphalocrocis medinalis,Noctuidae (owlet moths) such as Spodoptera litura, Pseudaletia separata,and Mamestra brassicae, Heliothis moths, Agrotis moths like Agrotisipsilon and Agrotis segetum (turnip moth), Pieridae such as Pieris rapaecrucivora, Tortricidae (bell moths), Lyonetiidae (leaf mining moths),Euproctis subflava, Plutella xylostella, Tinea translucens, Tineolabisselliella, etc.;

Diptera:

Culex (house mosquitos) such as Culex pipiens pallens and Culestritaeniorhynvchus, Aedes such as Aedes albopictus and Aedes aegypti,Anophelinae such as Anophelinae sinensis, Chironomidae (midges),Muscidae such as Musca domestica (house fly) and Muscina stabulans,Calliphoridae (blow flies), Sarcophagidae (flesh flies), Anthomyiidaesuch as Delia platura and Delia antigua, Trypetidae (fruit flies),Drosophilidae (wine flies), Psychodidae (moth flies), Tabanidae (deerflies), Simuliidae (black flies), Stomoxyinae, etc.;

Coleoptera (beetles):

Diabrotica (corn rootworms) such as Diabrotica virgifera and Diabroticaundecimunctata, Scarabaeidae such as Anomala cuprea and Anomalarufocuprea, Curculionidae (snout beetles) such as Sitophilus zeamais(grain weevils) and Lissorphoptrus oryzophilus, darkling beetles such asNeatus ventralis, Tenebrio molitor and Tribolium castaneum,Chrysomelidae (leaf beetles) such as Aulacophora femoralis andPhyllotreta striolata, Anobiidae (death-watch beetles), Epilachna suchas Henosepilachna vigintioctopunctata, Lyctidae (powder-post beetles),Bostrychidae (lesser grain borers), Paederus fuscipes, etc.;

Blattaria (cockroaches):

Blattella germanica, Periplaneta fuliginosa, Periplaneta americana,Periplaneta brunnea, Blatta orientalis, etc.;

Thysanoptera (thrips):

Thrips palmi, Thrips hawaiiensis, etc.;

Hymenoptera:

Formicidae (ants), Vespa (hornets), Bethylidae (bethylid wasps),Tenthredinidae (sawflies) like Athalia japonica (cabbage sawfly), etc.;

Orthoptera:

Gryllotalpa (mole crickets), Acrididea (grasshoppers), etc.;

Siphonaptera (fleas):

Purex irritans, etc.;

Anoplura (sucking louses):

Pediculus humanus, Phthirus pubis, etc.;

Isoptera (termites):

Reticulitermes speratus, Coptotermes formosanus, etc.;

Tetranychidae (spider mites):

Tetranychus cinnabarinus, Tetranychus urticae, Tetranychus kanzawai,Panonychus citri, Panonychus ulmi, etc.;

Ixodidae (ticks):

Boophilus microplus;

house dust mites:

Acaridae, Pyroglyphidae, Cheyletidae, Ornithonyssus bacoti, etc.;

Nematoda (soil nematodes):

root-lesion nematodes, cyst nematodes, root-knot nematodes, etc.; and

Nematoda (nematodes):

Bursaphelenchus xylophilus (pine wood nematodes), etc.

The present compound to be used as an active ingredient of aninsecticide, an acaricide, a nematicide or an active agent forcontrolling soil insect pests is usually formulated by mixing with asolid carrier, a liquid carrier, a gaseous carrier or bait, or issupported by a base material of a mosquito-coil or mosquito-mat forelectric heating fumigation through impregnation.

A surfactant, a sticking agent, a dispersion agent, a stabilizer andother auxiliaries or additives are added if necessary.

Examples of the formulations for the present compound include oilsolutions, emulsifiable concentrates, wettable powders, flowables suchas water suspensions and emulsions, granules, dusts, aerosols,combustible or chemical fumigants such as mosquito-coil, mosquito-matsfor electric heating fumigation and a porous ceramic fumigant, volatileagents applied on resin or paper, fogging agents, ULV agents(formulations for ultra low volume application) and poisonous bait.

These formulations usually include the present compound as an activeingredient in an amount of 0.001% to 95% by weight.

Examples of the solid carrier to be used for the formulations includefine powder or granules of clays (e.g. kaolin clay, diatomaceous earth,synthetic hydrated silicon oxide, bentonite, Fubasami clay and acidclay), talcs, ceramics, other inorganic minerals (e.g. sericite, quartz,sulfur, active carbon, calcium carbocarbonate and hydrated silica) andchemical fertilizers (e.g. ammonium sulfate, ammonium phosphate,ammonium nitrate, urea and ammonium chloride).

Examples of the liquid carrier include water, alcohols such as methanoland ethanol, ketones such as acetone and methylethyl ketone, aromatichydrocarbons such as benzene, toluene, xylene, ethylbenzene, andmethylnaphthalene, aliphatic hydrocarbons such as hexane, cyclohexane,kerosine, and gas oil, esters such as ethyl acetate and butyl acetate,nitriles such as acetonitrile and isobutyronitrile, ethers such asdiisopropyl ether and dioxane, acid amides such as N,N-dimethylformamideand N,N-dimethylacetoamide, halogenated hydrocarbons such asdichloromethane, trichloroethane, and carbon tetrachloride, dimethylsulfoxide, vegetable oils such as soybean oil and cottonseed oil.

Examples of the gaseous carrier or propellant include CFCs(chlorofluorocarbons), butane gas, LPG (liquefied petroleum gas),dimethyl ether and carbon dioxide.

Examples of the surfactant includes alkyl sulfates, alkyl sulfonates,aralkyl sulfonates, aralkyl ethers, poly(ethylene glycol)s, polyethyleneglycol ethers, polyhydric alcohol derivatives, and sugar alcoholderivatives.

Examples of the sticking agent, the dispersing agent and otherequivalent additives or auxiliaries include casein, gelatin,polysaccharides such as starch, gum arabic, cellulose derivatives andalginic acid, lignin derivatives, bentonite, sugars and syntheticwater-soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidoneand polyacrylic acid.

Examples of the stabilizer include PAP (acid isopropyl phosphate), BHT(2,6-di-t-butyl-4-methyl-phenol), BHA (mixture of2-t-butyl-4-methoxyphenol and 3-t-butyl-4-methoxyphenol), vegentableoils, mineral oils, surfactants, fatty acides and esters of fatty acids.

The base material of the mosquito-coil may be a mixture of raw plantpowder such as wood powder and lees powder, powder of Machilusthunbergii Sieb. et Zucc., and a binding agent like starch or gluten.

The base material of mosquito-mat for electric heating fumigation may bea plate of compacted fibrils of cotton linters or a mixture of pulp andcotton linters.

The base material of the combustible fumigant includes, for example, anexothermic agent such as a nitrate, a nitrite, a guanidine salt,potassium chlorate, nitrocellulose, ethylcellulose or wood powder, apyrolytic stimulating agent such as an alkaline metal salt, an alkalineearth metal salt, a dichromate or a chromate, an oxygen source such aspotassium nitrates, a combustion assistant such as melamine or wheatstarch, a bulk filler such as diatomaceous earth and a binding agentsuch as synthetic glue.

The base material of the chemical fumigant includes, for example, anexothermic agent such as an alkaline metal sulfide, a polysulfide, ahydrosulfide, a hydrated salt or calcium oxide, a catalytic agent suchas a carbonaneous substance, iron carbide or activated clay, an organicfoaming agent such as azodicarbonamide, benzenesulfonylhydrazide,N,N'-dinitrosopentamethylene, tetramine, polystyrene or polyurethane anda filler such as natural or synthetic fibers.

Examples of the base material of the volatile agent includethermoplastic resins, filter paper and rice paper.

The base material of the poisonous baits includes a bait component suchas grain powder, purified vegetable oil, sugar, or crystallinecellulose, an antioxidant such as dibutylhydroxytoluene ornordihydroguaiaretic acid, a preservative such as dehydroacetic acid, asubstance for preventing erroneous eating such as red pepper powder, anattractant such as cheese flavor, onion flavor or peanut oil.

The flowables (water suspensions and emulsions) are usually prepared byfinely dispersing the present compound at a ratio of 1 to 75% in watercontaining a 0.5 to 15% dispersing agent, a 0.1 to 10% suspensionassistant (for example, protective colloid or a compound givingthixotropy) and 0 to 10% additives (for example, an antifoamer, astabilizer, a bactericide, a rust preventive agent, an antimold, adeveloping agent, a penetrating assistant and an antifreezing agent).

The present compound may be dispersed in oil, in which the presentcompound is substantially insoluble, to form oil suspensions.

Examples of the protective colloid include casein, gelatin, gums,cellulose ethers and polyvinyl alcohol. The compound giving thixotropymay be bentonite, aluminum magnesium silicate, xanthan gum orpolyacrylic acid.

The formulations thus obtained is used as prepared or diluted with waterand may be used simultaneously with another insecticide, anotheracaricide, another nematicide, another soil insect controlling agent, abactericide, a herbicide, a plant growth regulator, a synergist, afertilizer or a soil conditioner under non-mixed conditions or pre-mixedconditions.

Insecticides, acaricides and nematocides to be used together with thepresent compounds include organophosphorous compounds such as

Fenitrothion (O,O-dimethyl O-(3-methyl-4-nitrophenyl)phosphorothionate!,

Fenthion O,O-dimethyl O-(3-methl-4-methylthiophenyl)phophorothionate!,

Diazinon (Dimpylate)O,O-diethyl-O-2-isopropyl-6-methylpyrimidin-4-ylphosphorothioate!,

Chlorpyriphos O,O-dimethyl-O-3,5,6-trichloro-2-pyridylphosphorothioate!,

Acephate O,S-dimethylacetylphosphoramidothioate!,

Methidachion (DMTP)S-2,3-dihydro-5-methoxy-2-oxo-1,3,4-thiadiazol-3-ylmethylO,O-dimethylphosphorothiolothionate!,

Disulfoton O,O-diethyl S-2-ethylthioethyl phosphorothiolothionate!,

Dichlorvos (DDVP) 2,2-dichlorovinyl dimethylphosphate!,

Sulprofos O-ethyl O-4-methylthiophenyl S-propyl phosphorodithioate!,

Cyanophos O-4-cyanophenyl-O,O-dimethylphosphorothioate!,

Dioxabenzofos 2-methoxy-4H-1,3,2-benzodioxaphosphorin 2-sulfide!,

Dimethoate O,O-dimethyl-S-(N-methylcarbamoylmethyl)phosphorodithioate!,

Phenthoate S-ethoxycarbonylbenzyldimethyl phosphorothiolothionate!,

Malathion 1,2-bis(ethoxylcarbonyl)-ethyl O,O-dimethylphosphorothiolothionate!,

Trichlorfon (Metrifonate) dimethyl 2,2,2-trichloro-1-hydroxyethylphosphonate!,

Azinphos-methylS-(3,4-dihydro-4-oxo-1,2,3-benzotriazine-3-ylmethyl)dimethylphosphorothiolothionate!,

Monocrotophos cis-3-(dimethoxyphosphinyloxy)-N-methylcrotonamide!and

Ethion O,O,O',O'-tetraethyl S,S'-methylene bis(phosphorodithioate)!.

Other examples are carbamate compounds such as

BPMC O-sec butyl(phenylmethylcarbamate!,

Benfuracarb ethylN-(2,3-dihydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio)-N-isopropyl-β-allaninate!,

Propoxur (PHC) 2-isopropoxy phenyl-N-methyl carbamate!,

Carbosulfan 2,3-dihydro-2,2-dimethyl-7-benzo b!furanylN-dibutylaminothio-N-methyl carbamate!,

Carbaryl 1-naphthyl-N-methylcarbamate!,

Methomyl S-methyl-N-((methylcarbamoyl)oxy)thioacetoimidate!,

Ethiofencarb 2-(ethylthiomethyl)phenyl methylcarbamate!,

Aldicarb 2-methyl-2-(methylthio)propanolO-((methylamino)carbonyl)oxime!,

Oxamyl N,N-dimethyl-2-methylcarbamoyloxyimino-2-(methylthio)acetamide!and

Fenothiocarb S-4-phenoxybutyl)-N,N-dimethylthiocarbamate!.

Other examples include pyrethroid compounds such as

Ethofenprox 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether!,

Fenvalerate (RS)-α-cyano-3-phenoxybenzyl(RS)-2-(4-chlorophenyl)-3-methylbutyrate!,

Esfenvalerate (S)-α-cyano-3-phenoxybenzyl(S)-2-(4-chlorophenyl)-3-methylbutyrate!,

Fenpropathrin (RS)-α-cyano-3-phenoxybenzyl2,2,3,3-tetramethylcyclopropanecarboxylate!,

Cypermethrin (RS)-α-cyano-3-phenoxybenzyl(1RS,3RS)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate!,

Permethrin 3-phenoxybenzyl(1RS,3RS)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate!,

Cyhalothrin (RS)-α-cyano-3-phenoxybenzyl(Z)-(1RS)-cis-3-(2-chloro-3,3,3-trifluoropropen-1-yl)-2,2-dimethylcyclopropanecarboxylate!,

Deltamethrin (S)-α-cyano-3-phenoxybenzyl(1R,3R)-3(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate!,

Cycloprothrin (RS)-α-cyano-3-phenoxybenzyl(RS)-2,2-dichloro-1-(4-ethoxyphenyl)cyclopropanecarboxylate!,

Fluvalinate α-cyano-3-phenoxybenzylN-(2-chloro-α,α,α-trifluoro-p-tolyl)-D-valinate!,

Bifenthrine 2-methylbiphenyl-2-ylmethyl)(Z)-(1RS)-cis-3-(2-chloro-3,3,3-trifluoropropen-1-yl)-2,2-dimethylcyclopropanecarboxylate!,

Acrinathrin (S)-(α)-cyano-(3-phenoxyphenyl)methyl(1R)-(1(S*),3α(Z))-2,2-dimethyl-3-(3-oxo-3-(2,2,2-trifluoro-1-(trifluoromethyl)ethoxy-1-propenyl)cyclopropanecarboxylate!,

2-methyl-2-(4-bromodifluoromethoxyphenyl)propyl (3-phenoxybenzyl)ether,

Traromethrin (S)-α-cyano-3-phenoxylbenzyl(1R,3R)-3-((1'RS)(1',1',2',2'-tetrabromoethyl))-2,2-dimethylcyclopropanecarboxylate!and

Silafluofen4-ethoxylphenyl-(3-(4-fluoro-3-phenoxyphenyl)propyl)dimethylsilane!.

Other examples include thiadiazine derivatives such as

Buprofezin 2-t-butylimino-3-isopropyl-5-phenyl-1,3,5-thiadiazin-4-one!,

nitroimidazolidine derivatives such as

Imidachloprid1-(6-chloro-3-pyridylmethl)-N-nitroimidazolidine-2-indenamine!,

Cartap S,S'-(2-dimethylaminotrimethylene)bisthiocarbamate!,

Thiocyclam N,N-dimethyl-1,2,3-trithian-5-ylamine!,

Bensultap S,S'-2-dimethylaminotrimethylene di(benzenethiosulfonate)!,

N-cyanoamidine derivatives such asN-cyano-N'-methyl-N'-(6-chloro-3-pyridylmethyl)acetoamidine,

chlorinated hydrocarbons such as Endosulfan

6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methanobenzoe!-2,4,3-dioxathiepin 3-oxide!,

γ-BHC 1,2,3,4,5,6-hexachlorocyclohexane!,

1,1-bis(chlorophenyl)-3,3,3-trichloroethanol,

benzoylphenyl urea compounds such as

Chlorofluazuron1-(3,5-dichloro-4-(3-chloro-5-trifluoromethylpyrid-2-yloxy)phenyl)-3-(2,6-difluorobenzoyl)urea!,

Teflubenzuron1-(3,5-dichloro-2,4-difluorophenyl)-3-(2,6-difluorobenzoyl)urea! and

Flufenoxron1-(4-(2-chloro-4-trifluoromethylphenoxy)-2-fluorophenyl)-3-(2,6-difluorobenzoyl)urea!,

formamidine derivatives such as

AmitrazN'-(2,4-dimethylphenyl)-N-((2,4-dimethylphenyl)imino)methyl)-N-methylmethanimidamide!and

Chlordimeform N'-(4-chloro-2-methylphenyl)-N,N-dimethylmethanimidamide!,

thio-urea derivatives such as

DiaphenthiuronN-(2,6-diisopropyl-4-phenoxyphenyl)-N'-t-butylcarbodiimide!,

Bromopropylate isopropyl 4,4'-dibromobenzilate!,

Tetradifon 2,4,5,4'-tetrachlorodiphenylsulfone!,

Quinomethionate 6-methyl-2-oxo-1,3-dithiolo-(4,6-b)-quinoxaline!,

Propargite 2-(4-(1,1-dimethylethyl)phenoxy)-cyclohexyl2-propynylsulfite!,

Fenbutatin oxide bis(tris(2-methyl-2-phenylpropyl)tin)oxide!,

Hexythiazox(4RS,5RS)-5-(4-chlorophenyl)-N-chlorohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide!,

Chlofentezine 3,6-bis(2-chlorophenyl)-1,2,4,5-tetrazine!, Pyridathioben2-t-butyl-5-(4-t-butylbenzylthio)-4-chloropyridazin-3(2H)-on!,

Phenpyroxymatet-butyl(E)-4-((1,3-dimethyl-5-phenoxypyrazol-4-yl)methyleneaminooxymethyl)benzoate!,

DebphenpyradN-4-t-butylbenzyl-4-chloro-3-ethyl-1-methyl-5-pyrazolcarboxamide!,

polynactin complexes including tetranactin, trinactin, dinactin,Milbemectin, Avermectin, Ivermectin and Azadilactin, and

Pyrimidifen5-chloro-N-(2-(4-(2-ethoxyethyl)-2,3-dimethylphenoxy)ethyl)-6-ethylpyrimidine-4-amine!.

When the present compound is applied as an active ingredient ofinsecticides, nematocides, and acaricides for agricultural use andactive agents for controlling soil insect pests, the amount ofapplication is generally 5 to 500 g per 1,000 m².

Emulsifiable concentrates, wettable powders and flowables such as watersuspensions and emulsions are diluted with water to the concentration of0.1 to 1000 ppm.

Granules and dusts are not diluted but used as prepared. When thepresent compound is applied as an active ingredient of insecticides andacaricides for house-hold use, emulsifiable concentrates, wettablepowders and flowables are diluted with water to the concentration of 0.1to 10000 ppm.

Oil solutions, aerosols, fumigants, volatile agents, fogging agents, ULVagents (formulations for ultra low volume applications), and poisonousbaits are used as prepared.

The amount and concentration of application may be varied optionallyaccording to the type of the formulations, time, place, and method ofapplication, the type of noxious insect pests and the damage.

The invention will be further illustrated in detail by the productionexamples, formulation examples and biological tests although theinvention is not limited in any sense to these examples.

EXAMPLE 1

540 mg of(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylicacid chloride was added under ice-water cooling to a mixed solution of400 mg of (RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-ol, 5 mgof 2,6-di-t-butyl-4-methylphenol and 274 mg of pyridine in 6 ml oftoluene. The reaction was allowed to react at an ambient temperature foreight hours. The reaction solution was added to a 5% citric acidsolution under ice-water cooling and extracted three times with diethylether. The combined ether layer was washed successively with a saturatedsodium hydrogencarbonate solution and a saturated sodium chloridesolution and dried over anhydrous magnesium sulfate. After removal ofthe solvent under reduced pressure, the obtained residue was subjectedto silica gel column chromatography to yield 751 mg of(RS)-2-methyl-4-methylidene-3-ethyl-2-cyclopenten-1-yl(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate(Compound No.1). Yield 72% (Eluent: n-hexane/ethyl acetate=30/1,2,6-di-t-butyl-4-methylphenol 0.1%) n_(D) ²⁰.5 1.5070

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.05 (m, 3H),1.11 (m, 3H), 1.27 (m, 3H), 1.41 (m, 1H), 1.70 (s, 6H), 1.79 (s, 3H),2.05 (m, 1H), 2.15-2.49 (m, 3H), 2.90-3.10 (m, 1H), 4.75 (m, 1H),4.70-4.96 (m, 2H), 5.50-5.71 (m, 1H).

IR (neat) ν_(max) (cm⁻¹): 1194, 1232, 1636, 1724, 2880, 2940, 2976

EXAMPLE 2

625 mg of(1R)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acidchloride was added under ice-water cooling to a mixed solution of 400 mgof (RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-ol, 5 mg of2,6-di-t-butyl-4-methylphenol and 274 mg of pyridine in 6 ml of toluene.The reaction was continued at an ambient temperature for eight hours.The reaction solution was added to a 5% citric acid solution underice-water cooling, and extracted three times with diethyl ether. Thecombined ether layer was washed successively with a saturated sodiumhydrogencarbonate solution and a saturated sodium chloride solution, anddried over anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the residue was subjected to silica gel columnchromatography to yield 781 mg of(RS)-2-methyl-4-methylidene-3-ethyl-2-cyclopenten-1-yl(1R)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate(Compound No.5). Yield 82%. (Eluent: n-hexane/ethyl acetate=30/1,2,6-di-t-butyl-4-methylphenol 0.1%) n_(D) ²³ 1.5251

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.04 (t, 3H),1.19 (m, 3H), 1.29 (m, 4H), 1.62 (m, 1H), 1.80 (d, 3H), 2.11-2.52 (m,3H), 2.88-3.10 (m, 1H), 4.78 (m, 1H), 4.87 (m, 1H), 5.53-5.75 (m, 2H)

EXAMPLE 3

Under ice-water cooling, 0.26 g of(1R)-cis,trans-2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropanecarboxylicacid chloride was added dropwise to the solution of 0.21 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ol and 0.14ml of pyridine in 5 ml of toluene and then stirred at an ambienttemperature for six hours. The reaction solution was poured intoice-water and extracted with ethyl acetate. The ethyl acetate layer waswashed successively with 5% aqueous hydrochloric acid, water and asaturated sodium chloride solution, and dried over anhydrous magnesiumsulfate. After removal of the solvent under reduced pressure, theobtained oily substance was subjected to silica gel columnchromatography to yield 0.26 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopenten-2-yl(1R)-cis,trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate(Compound No.2). Yield 61% n_(D) ²³ 1.5076

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.12-2.04 (m,17H), 2.51 (m, 1H), 3.04 (m, 1H), 3.16 (m, 1H), 4.87-5.11 (m, 5H),5.36-5.95 (m, 3H).

IR (neat) ν_(max) (cm⁻¹): 3092, 2976, 2936, 2880, 1726, 1642, 1614,1452, 1424, 1380, 1318, 854

EXAMPLE 4

After 0.21 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ol wasdissolved in 5 ml of toluene, 0.14 ml of pyridine was added to thetoluene solution. Under ice-water cooling, 70%(w/w) toluene solutioncontaining 0.32 g of 2,2,3,3-tetramethylcyclopropanecarboxylic acidchloride was added dropwise to the mixed solution, and then stirred atan ambient temperature for six hours. The reaction solution was pouredinto ice-water and extracted with ethyl acetate. The ethyl acetate layerwas washed successively with 5% aqueous hydrochloric acid and water, andvigorously stirred with 5% ammonia water for two hours. The ethylacetate layer was then washed with a saturated sodium chloride solutionand dried over anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the obtained oily substance was subjected tosilica gel column chromatography to yield 0.24 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopenten-2-yl2,2,3,3-tetramethylcyclopropanecarboxylate (Compound No.12). Yield 62%n_(D) ²³ 1.5023

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.16-1.27 (m,13H), 1.79 (s, 3H), 2.38 (m, 1H), 3.01 (m, 3H), 4.76 (s, 1H), 4.85 (s,1H), 5.03 (m, 2H), 5.60 (brd, 1H), 5.78 (m, 1H).

IR (neat) ν_(max) (cm⁻¹): 3092, 2952, 1726, 1642, 1614, 1454, 1414,1396, 1382, 1326, 844

EXAMPLE 5

After 0.26 g of (RS)-3-isopropyl-4-methylidenecyclopent-2-en-1-ol wasdissolved in 5 ml of toluene, 0.23 ml of pyridine was added to thetoluene solution. Under ice-water cooling, 0.55 g of(1RS)-cis-3-(Z-2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride was added dropwise to the mixed solution, and then stirredat an ambient temperature for six hours. The reaction solution waspoured into ice-water and extracted with ethyl acetate. The ethylacetate layer was washed successively with 5% aqueous hydrochloric acid,water, and a saturated sodium chloride solution, and dried overanhydrous magnesium sulfate. After removal of the solvent under reducedpressure, the obtained oily substance was subjected to silica gel columnchromatography to yield 0.25 g of(RS)-3-isopropyl-4-methylidenecyclopenten-2-yl(1RS)-cis-3-(Z-2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate(Compound No.6). Yield 39% n_(D) ²⁶ 1.4804

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.14 (m, 6H),1.24-1.32 (m, 6H), 1.95 (d, 1H), 2.12 (m, 1H), 2.44-2.66 (m, 2H),2.96-3.09 (m, 1H), 4.93 (s, 1H), 5.01 (s, 1H), 5.64 (m, 1H), 5.86 (s,1H), 6.93 (m, 1H)

IR (neat) ν_(max) (cm⁻¹): 3092, 2972, 2884, 1726, 1652, 1616, 1464,1416, 1382, 1338, 868

EXAMPLE 6

Under ice-water cooling, 350 mg of(1R)-trans-3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride was added dropwise to the mixed solution of 300 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-ol,5 mg of 2,6-di-tert-butyl-4-methylphenol, 185 mg of pyridine and 5 mg of4-dimethylaminopyridine in 10 ml of dry terahydrofuran and then theresultant reaction mixture was allowed to react further 6 hours at roomtemperature. Then 10 ml of 10% aqueous ammonia solution was added to thesolution and vigorously stirred for 2 hours. The reaction mixture wasextracted three times with diethyl ether and the ether layers werecombined. The combined layer was washed with brine and dried overanhydrous magnesium sulfate. After removal of the drying agent, thesolvent was evaporated. The obtained residue was subjected to silica gelcolumn chromatography to afford 280 mg of the desired(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-yl(1R)-trans-3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylate(Compound No.15). Yield 52% (Eluent: n-hexane/ethyl acetate=30/1,2,6-di-tert-butyl-4-methylphenol 0.1% ) n_(D) ²¹ 1.4805

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.14 (m, 3H),1.28 (m, 3H), 1.40 (m, 1H), 1.71 (m, 6H), 1.85 (d, 3H), 2.08 (m, 1H),2.43 (m, 1H), 3.07 (m, 3H), 4.88 (m, 3H), 5.63 (brd, 0.5H), 5.70 (brd,0.5H)

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ values (ppm): -64.35 (t,3F).

EXAMPLE 7

430 mg of(1R)-trans-2,2-domethyl-3-(2,2-dichlorovinyl)cyclopropanecarboxylic acidchloride was used instead of(1R)-trans-3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride in Example 6 above and the reaction procedures werecarried out in a similar manner as in the example 6 to afford 410 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-yl(1R)-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropanecarboxylate(Compound No. 54). Yield 69% n_(D) ²¹ 1.4999

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.19 (m, 3H),1.30 (m, 3H), 1.62 (m, 1H), 1.75 (d, 3H), 2.23 (m, 1H), 2.46 (m, 1H),3.07 (m, 3H), 4.91 (d, 2H), 5.63 (m, 1.5H), 5.72 (brd, 0.5H).

¹⁹ F-NMR (CDCl₃ internal standard CCl₃ F) δ values (ppm): -64.33(t, 3F).

EXAMPLE 8

A 70% toluene solution containing 430 mg of2,2,3,3-tetramethylcyclopropanecarboxylic acid chloride was used insteadof (1R)-trans-3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride in Example 6 above and the reaction procedures werecarried out in a similar manner as in Example 6 to afford 345 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-yl2,2,3,3-tetramethylcyclopropanecarboxylate (Compound No. 43). Yield 70%n_(D) ²⁴ 1.4687

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.25 (m, 13H),1.85 (s, 3H), 2.43 (m, 1H), 3.07 (m, 3H), 4.88 (d, 2H), 5.65 (brd, 1H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ values (ppm): -64.31(t,3F).

EXAMPLE 9

370.25 mg of (2S)-2-(4-fluorophenyl)-3-methylbutyryl chloride was usedinstead of(1R)-trans-3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride in Example 6 above and the reaction procedures werecarried out in a similar manner as in Example 6 to afford 430 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-yl(2S)-2-(4-fluorophenyl)-3-methylbutyrate (Compound No. 72). Yield 78%n_(D) ²³ 1.4879

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.71 (m, 3H),1.08 (d, 3H), 1.71 (d, 2H), 2.34 (m, 2H), 3.01 (m, 3H), 3.12 (d, 1H),4.88 (m, 2H), 5.68 (m, 1H), 7.00 (m, 2H), 7.30 (m, 2H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ values (ppm): -116.01 (s,1F), -64.32 (t, 3F).

EXAMPLE 10

After 0.20 g of (RS)-3-isopropyl-4-methylidenecyclopent-2-en-1-ol wasdissolved in 5 ml of toluene, 0.15 ml of pyridine was added to thetoluene solution. Under ice-water cooling, 0.31 g of(1R)-trans-3-(2-chloro-2-fluoroethenyl)-2,2-dimethylcyclopropanecarboxylicacid chloride was added dropwise to the mixed solution, and then stirredat an ambient temperature for six hours. The reaction solution waspoured into ice-water and extracted with ethyl acetate.

The ethyl acetate layer was washed successively with 5% aqueoushydrochloric acid and water, then vigorously stirred with 5% ammoniawater for two hours. The ethyl acetate layer was then washed with asaturated sodium chloride solution and dried over anhydrous magnesiumsulfate. After removal of the solvent under reduced pressure, theobtained oily substance was subjected to silica gel columnchromatography to yield 0.27 g of(RS)-3-isopropyl-4-methylidenecyclopenten-2-yl(1R)-trans-3-(2-chloro-2-fluoroethenyl)-2,2-dimethylcyclopropanecarboxylate(Compound No.17). Yield 60% n_(D) ²³.5 1.5014

¹ H-NMR (CDCl₃ internal standard TMS) δ values (ppm): 1.11-1.28 (m,12H), 1.50 (m, 1H), 1.97-2.23 (m, 1H), 2.43-2.66 (m, 2H), 2.97-3.10 (m,1H), 4.63 (dd, 0.5H), 5.08 (dd, 0.5H), 4.92 (s, 1H), 5.00 (s, 1H), 5.66(m, 1H), 5.88 (m, 1H).

IR (neat) ν_(max) (cm⁻¹): 3092, 2972, 2880, 1726, 1676, 1640, 1616,1462, 1430, 1382, 1360, 1336, 850

EXAMPLE 11

823 mg of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride(WSC) was added to a solution of 500 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-ene-1-ol,500 mg of(1R)-trans-2,2-dimethyl-3-((E)-2-methoxycarbonyl-1-propenyl)cyclopropanecarboxylicacid and 580 mg of triethylamine in 10 ml of dichloromethane underice-water cooling. The resulting reaction mixture was further allowed toreact for 8 hours at room temperature. Then the reaction solution waspoured into an ice-cooled 5% aqueous citric acid solution, and extractedthree times with diethyl ether. The combined ether layer was washed withsaturated sodium hydrogen carbonate and saturated sodium chloridesolution, after dried over anhydrous magnesium sulfate, the solvent wasevaporated under reduced pressure. The obtained residue was subjected tosilica gel column chromatography to afford 823 mg of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)-2-cyclopent-1-yl(1R)-trans-2,2-dimethyl-3-((E)-2-methoxycarbonyl-1-propenyl)-cyclopropanecarboxylate(Compound No. 70). n_(D) ²² 1.4940

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.25 (d, 3H),1.32 (d, 3H), 1.73 (m, 1H), 1.87 (d, 3H), 1.93 (s, 3H), 2.22 (m, 1H),2.45 (m, 1H), 3.06 (m, 3H), 3.72 (s, 3H), 4.91 (d, 2H), 5.64 (brd,0.5H), 5.76 (brd, 0.5H), 6.48 (d, 1H)

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ value (ppm): -64.35 (t, 3F)

EXAMPLE 12

A mixture of 12.5 ml of ether, 1.0 ml of t-butanol and 3.85 g oftriphenylmethylphosphonium bromide was stirred at an ambienttemperature, then 1.21 g of potassium t-butoxide was added to themixture and stirred at an ambient temperature for five hours. Underice-water cooling, 1.64 g of(RS)-3-(1-methyl-2-propenyl)4-oxocyclopent-2-en-1-ol dissolved in 2.0 mlof ether was added dropwise to the mixed solution and stirred for twohours. The mixture was subsequently stirred at an ambient temperaturefor six hours. The reaction solution was poured into a saturated aqueoussodium dihydrogen phosphate solution and extracted with ether. Theorganic layer was washed with a saturated sodium chloride solution, anddried over anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the obtained oily substance was subjected tosilica gel column chromatography to yield 0.20 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ol. Yield 12%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.24 (t, 3H),1.56 (brs, 1H), 2.43 (m, 1H), 3.00 (m, 1H), 3.15 (m, 1H), 4.80-5.10 (m,5H), 5.79-5.95 (m, 2H).

EXAMPLE 13

2.02 Grams of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ylt-butyldimethylsilyl ether was dissolved in 20 ml of tetrahydrofuran.Under ice-water cooling, 7.7 ml of a tetrahydrofuran solution of 1Mn-tetrabutylammonium fluoride was added to the ether solution, and thenstirred at an ambient temperature for six hours. The reaction solutionwas poured into ice-water and extracted with ether. The ether layer waswashed with a saturated sodium chloride solution, and dried withanhydrous magnesium sulfate. After removal of the solvent under reducedpressure, the oily substance obtained was subjected to silica gel columnchromatography to yield 1.05 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ol. Yield 91%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.24 (t, 3H),1.56 (brs, 1H), 2.42 (m, 1H), 2.99 (m, 1H), 3.15 (m, 1H), 4.81-5.10 (m,5H), 5.80-5.95 (m, 2H)

EXAMPLE 14

Under stirring, 9.65 g of potassium t-butoxide was added over 10 minutesto a mixed solution of 7 g of t-butanol and 30.7 g oftriphenylmethylphosphonium bromide in 85 ml of diethyl ether. The mixedsolution was allowed to react at an ambient temperature for eight hours,and then cooled to 0° C. A solution prepared by dissolving 9 g of(RS)-4-hydroxy-3-methyl-2-ethylcyclopent-2-en-1-one in 10 ml of diethylether was added to the mixed solution over 10 minutes. After thereaction solution was warmed over two hours from 0° C. to the roomtemperature, the solution was further allowed to react for eight hours.The reaction solution was then added to 100 ml of a saturated aqueoussodium dihydrogen phosphate solution, and extracted three times with 100ml of diethyl ether. The combined organic layer was dried over anhydrousmagnesium sulfate. After removal of the solvent under reduced pressure,the residue was dissolved in ether, stirred for two minutes, andfiltered through Celite (registered trade mark by Johns-Manville). Thefiltrate was concentrated under reduced pressure, and the residueobtained was treated by silica gel column chromatography to yield 5.8 gof (RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-one. Yield 65%(Eluent: n-hexane/ethyl acetate=5/1 (v/v))

¹ H-NMR (CDCl₃ internal standard TMS) δ values (ppm): 1.02 (t, 3H), 1.42(m, 1H), 1.82 (s, 3H), 2.20 (q, 2H), 2.31 (m, 0.5H), 2.38 (m, 0.5H),2.87-3.01 (m, 1H), 4.58 (m, 1H), 4.72 (m, 1H), 4.81 (m, 1H)

EXAMPLE 15

After 4.0 g of(RS)-2-methyl-4-methylidene-3-ethyl-1-t-butyldimethylsilyloxy-2-cyclopentenewas dissolved in 35 ml of dry tetrahydrofuran, 17.5 ml of a 1Mtetrabutylammonium fluoride/tetrahydrofuran solution was added undercooling and stirred at ambient temperatures for twelve hours. Thereaction solution was then added to 100 ml of an ice-cooled 5% aqueousoxalic acid, and extracted with diethyl ether (300 ml×3 times). Thecombined ether layer was washed successively with a saturated sodiumhydrogencarbonate solution and a saturated sodium chloride solution, anddried over anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the residue was treated by silica gel columnchromatography (eluent: n-hexane:ethyl acetate=3:1 (v/v)) to yield 2.0 gof (RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-ol. Yield 92%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.02 (t, 3H),1.42 (m, 1H), 1.82 (s, 3H), 2.02 (q, 2H), 2.31 (m, 0.5H), 2.38 (m,0.5H), 2.87-3.01 (m, 1H), 4.58 (m, 1H), 4.72 (m, 1H), 4.81 (m, 1H).

EXAMPLE 16

After 10.5 g of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)-1-t-butyldimethylsilyloxy-2-cyclopentenewas dissolved in 50 ml of dry tetrahydrofuran, a mixture of 10.5 ml of a1M tetrabutylammonium fluoride/tetrahydrofuran solution and 5 ml ofhydrofluoric acid was added under cooling and stirred at ambienttemperatures for twelve hours. The reaction solution was then added to100 ml of an ice-cooled 5% aqueous oxalic acid, and extracted withdiethyl ether (300 ml×3 times). The combined ether layer was washedsuccessively with a saturated sodium hydrogencarbonate solution and asaturated sodium chloride solution, and dried over anhydrous magnesiumsulfate. After removal of the solvent under reduced pressure, theresidue was treated by silica gel column chromatography (eluent:n-hexane:ethyl acetate=3:1 (v/v)) to yield 5.27 g of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)cyclopent-2-en-1-ol.Yield 80%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.91 (s, 3H),2.43 (m, 1H), 3.02 (m, 3H), 4.18 (brs, 1H), 4.85 (d, 2H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ value (ppm): -64.37 (t, 3F)

EXAMPLE 17

A suspension prepared by suspending 3.7 g of zinc dust in 30 ml oftetrahydrofuran was mixed with 1.4 ml of dibromomethane in an atmosphereof argon at a temperature of -20° to -10° C. After stirring for fifteenminutes, 12.5 ml of a dichloromethane solution of 1M titaniumtetrachloride was added dropwise to the suspension and stirred at theabove temperatures for thirty minutes and at 4° C. for three days. Asolution prepared by dissolving 3.33 g of(RS)-3-(1-methyl-2-propenyl)-4-oxocyclopent-2-en-1-ylt-butyldimethylsilyl ether in 15 ml of dichloromethane was addeddropwise to the reaction solution in an atmosphere of argon at atemperature of -20° to -10° C. After stirring at an ambient temperaturefor six hours, 30 ml of hexane was further added to the reactionsolution. Under stirring, a suspension prepared by suspending 15 g ofsodium hydrogencarbonate in 100 ml of water was added gradually to thereaction solution. After stirring at an ambient temperature for twohours, the reaction solution was filtered through celite, extracted withhexane, and dried over anhydrous magnesium sulfate. After removal of thesolvent under reduced pressure, the obtained oily substance wassubjected to silica gel column chromatography to yield 2.02 g of(RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-ylt-butyldimethylsilyl ether. Yield 61%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.08 (d, 6H),0.90 (s, 9H), 1.23 (dd, 3H), 2.42 (m, 1H), 2.92 (m, 1H), 3.12 (m, 1H),4.81-5.11 (m, 5H), 5.79-5.97 (m, 2H).

EXAMPLE 18

13.04 Grams of dibromomethane and 14.71 g of zinc dust were mixed in 120ml of dried tetrahydrofuran and cooled to 0° to 5° C. After 50 ml of adichloromethane solution of 1M titanium tetrachloride was added dropwiseto the mixed solution over fifteen minutes, the reaction was continuedat a temperature of 0° to 5° C. for three days.

A solution prepared by 12.67 g of(RS)-4-t-butyldimethylsilyloxy-3-methyl-2-ethylcyclopent-2-en-1-one in50 ml of dichloromethane was added dropwise to the reaction solution atthe temperatures of 0° to 5° C. over fifteen minutes. After the reactionwas run at the same temperatures for one hour, a mixture of 10 mg of2,6-di-t-butyl-4-methylphenol and 100 ml of hexane and slurry containing105 g of sodium hydrogencarbonate and 70 ml of water were successivelyadded to the reaction solution.

After stirring at a temperature of 0° to 5° C. for two hours, theorganic layer was decanted and the residue was extracted three timeswith 150 ml of n-hexane. The combined organic layer was washed with asaturated sodium hydrogencarbonate solution, and dried over anhydrousmagnesium sulfate. After removal of the solvent under reduced pressure,the residue was subjected to silica gel column chromatography to yield7.71 g of(RS)-2-methyl-4-methylidene-3-ethyl-1-t-butyldimethylsilyloxy-2-cyclopentene.Yield 62% (Eluent: n-hexane/ethyl acetate=20/1 (v/v))

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.1 (m, 6H), 0.89(s, 9H), 1.00 (s, 3H), 1.75 (s, 3H), 2.19 (q, 2H), 2.25-2.40 (m, 1H),2.78-2.91 (m, 1H), 4.64 (m, 2H), 4.73 (m, 1H).

EXAMPLE 19

10.01 Grams of dibromomethane and 11.51 g of zinc dust were mixed in 100ml of dried tetrahydrofuran and cooled to -40° C. After 4.52 ml oftitanium tetrachloride was added dropwise to the mixed solution over twominutes, the reaction was continued at a temperature of 0° to 5° C. forthree days.

A solution prepared by 12.34 g of(RS)-4-t-butyldimethylsilyloxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-onein 20 ml of dichloromethane was added dropwise to the reaction solutionat the temperature. After the reaction was run at the same temperaturesfor one hour, a mixture of 10 mg of 2,6-di-t-butyl-4-methylphenol and100 ml of hexane and slurry containing 105 g of sodium hydrogencarbonateand 70 ml of water were successively added to the reaction solution.

After stirring at a temperature of 0° to 5° C. for two hours, theorganic layer was decanted and the residue was extracted three timeswith 150 ml of n-hexane. The combined organic layer was washed with asaturated sodium hydrogencarbonate solution, and dried over anhydrousmagnesium sulfate. After removal of the solvent under reduced pressure,the residue was subjected to silica gel column chromatography to yield10.5 g of(RS)-2-methyl-4-methylidene-3-(2,2,2-trifluoroethyl)-1-t-butyldimethylsilyloxy-2-cyclopentene.Yield 85.7% (Eluent: n-hexane/ethyl acetate=20/1 (v/v))

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.08 (d, 6H),0.92 (s, 9H), 1.83 (s, 3H), 2.42 (m, 1H), 2.91 (m, 1H), 3.01 (q, 2H),4.71 (brs, 1H), 4.78 (d, 2H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ value (ppm): -64.42 (t, 3F)

EXAMPLE 20

1.43 Grams of imidazole was added to a solution prepared by dissolving2.71 g of (RS)-3-(1-methyl-2-propenyl)-4-oxo-2-cyclopent-2-en-1-ol in 30ml of N,N-dimethylformamide. Under ice-water cooling, 2.95 g oft-butyldimethylsilyl chloride was added to the mixed solution withstirring. After stirring at ambient temperatures for six hours, thereaction solution was poured into icy cold water and extracted withether. The ether layer was washed successively with 10% aqueous citricacid and a saturated sodium chloride solution, and dried over anhydrousmagnesium sulfate. After removal of the solvent under reduced pressure,the obtained oily substance was subjected to silica gel columnchromatography to yield 3.33 g of(RS)-3-(1-methyl-2-propenyl)-4-oxocyclopent-2-en-1-ylt-butyldimethylsilyl ether. Yield 70%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.10-0.12 (m,6H), 0.91 (s, 9H), 1.20 (t, 3H), 2.28 (dd, 1H), 2.75 (dd, 1H), 3.24 (m,1H), 4.88 (m, 1H), 5.00-5.10 (m, 2H), 5.86 (m, 1H), 7.01 (m, 1H).

EXAMPLE 21

After 10 g of(RS)-4-hydroxy-3-methyl-2-ethylcyclopent-2-en-1-one and5.78 g of imidazole were dissolved in 100 ml of dry dimethylformamide,11.91 g of t-butyldimethylchlorosilane was added to the solution at anambient temperature. After stirring at an ambient temperature for 14hours, the reaction solution was added to 5% aqueous citric acid underice-water cooling, and extracted three times with diethyl ether. Thecombined organic layer was washed successively with a saturated sodiumhydrogencarbonate solution and a saturated sodium chloride solution, anddried with anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the residue was subjected to silica gel columnchromatography to yield 14.231 g of(RS)-4-t-butyldimethylsilyloxy-3-methyl-2-ethylcyclopent-2-en-1-one.Yield 82% (Eluent: n-hexane/ethyl acetate=5/1 (v/v))

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.11 (m, 6H),0.91 (s, 9H), 1.00 (t, 3H), 2.01 (s, 3H), 2.12-2.31 (m, 3H), 2.69 (dd,1H), 4.65 (m, 1H).

EXAMPLE 22

After 10 g of(RS)-4-hydroxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-one and4.2 g of imidazole were dissolved in 100 ml of dry dimethylformamide,8.54 g of t-butyldimethylchlorosilane was added to the solution at anambient temperature. After stirring at an ambient temperature for 12hours, the reaction solution was added to 5% aqueous citric acid underice-water cooling, and extracted three times with diethyl ether. Thecombined organic layer was washed successively with a saturated sodiumhydrogencarbonate solution and a saturated sodium chloride solution, anddried with anhydrous magnesium sulfate. After removal of the solventunder reduced pressure, the residue was subjected to silica gel columnchromatography to yield 14.3 g of(RS)-4-t-butyldimethylsilyloxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-one.Yield 90% (Eluent: n-hexane/ethyl acetate=5/1 (v/v))

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 0.14 (d, 6H),0.92 (s, 9H), 2.12 (s, 3H), 2.30 (dd, 1H), 2.81 (dd, 1H), 3.08 (m, 2H),4.78 (brd, 1H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ value (ppm): -65.07 (t, 3F)

Preparation of (RS)-4-hydroxy-3-methyl-2-ethylcyclopent-2-en-1-one

1. Under an atmosphere of nitrogen, 10 ml of tetrahydrofuran and 10 mgof iodine were mixed with 3.974 g of magnesium flakes. With stirring, 3ml of a solution prepared by dissolving 22.28 g of ethyl bromide in 25ml of tetrahydrofuran was added dropwise to the mixture. The residualtetrahydrofuran solution of ethyl bromide was added dropwise to thereaction vessel placed in a water bath over one hour. After stirring forthirty minutes, a solution prepared by dissolving 15 g of5-methyl-2-furaldehyde in 5 ml of tetrahydrofuran was added dropwise tothe reaction solution over five minutes under ice-water cooling. Afterone hour, the reaction solution was added to a cooled 10% ammoniumchloride solution and stirred for five minutes. The mixed solution wasextracted twice with diethyl ether. The combined ether layer was washedtwice with a saturated sodium chloride solution, and dried overanhydrous magnesium sulfate. After removal of the solvent under reducedpressure, the residue was distilled, and a distillate fraction of 95° to98° C. at 22 mmHg was collected to yield 28.977 g of1-(5-methyl-2-furyl)propanol. Yield 91% b.p.: 95°-98° C. (22 mmHg)

¹ H-NMR (CDCl₃, solvent, internal standard TMS) δ values (ppm): 0.97 (t,3H), 1.78-2.02 (m, 3H), 2.29 (s, 3H), 4.51 (m, 1H), 5.89 (d, 1H), 6.11(d, 1H).

2. A mixed solution of 28.97 g of the 1-(5-methyl-2-furyl)propanol thusobtained, 0.394 g of 50% aqueous acetic acid, 0.394 g of a 23% (w/v)sodium hydroxide solution in 579.4 g of water was heated and refluxed atthe constant pH of 5.70 to 5.85 for 38 hours. After the mixed solutionwas cooled to the room temperature, a 23% (w/v) sodium hydroxidesolution was added to the mixed solution to adjust the pH of thesolution to 8.0 to 8.2, and then refluxed for three hours. A 50% aceticacid solution was added to the refluxing solution to adjust the pH to6.0 to 6.5. The reaction solution was then cooled to the roomtemperature, mixed with 300 g of sodium chloride, and extracted threetimes with 500 ml of diethyl ether. The combined ether layer was washedtwice with a saturated sodium chloride solution and dried over anhydrousmagnesium sulfate. After removal of the solvent under reduced pressure,the residue was distilled, and a distillate fraction of 157° to 162° C.at 19 mmHg was collected to yield 15 g of(RS)-4-hydroxy-3-methyl-2-ethylcyclopent-2-en-1-one. Yield 52% b.p.:157°-162° C. (19 mmHg)

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.01 (t, 3H),1.92 (m, 1H), 2.08 (s, 3H), 2.21 (q, 2H), 2.26 (dd, 1H), 2.78 (dd, 1H),4.71 (m, 1H).

Preparation of(RS)-2-methyl-3-(2,2,2-trifluoroethyl)-4-oxocyclopent-2-en-1-ol

1. A mixed solution of 123 g of potassium hydroxide, 900 ml of methanoland 80 ml of water was added to 160 g of ethyl 4,4,4-trifluorobutylatewith stirring under ice-water cooling and then the reaction mixture wasallowed to react for 12 hours at room temperature. The resultantreaction solution was concentrated under reduced pressure to obtain aresidue, which was then partitioned between water and diethyl ether. Theseparated ether layer was once washed with water and the separatedaqueous layer was combined with the previously obtained aqueous layer.An ice-cooled 10% hydrochloric acid solution was added to the combinedaqueous solution so that the pH of the solution was 1. Then the acidicsolution was extracted three times with diethyl ether. The layers werecombined and washed twice with brine, and dried over anhydrous magnesiumsulfate. The filtered solution was evaporated under reduced pressure toyield 131 g of the desired 4,4,4-trifluorobutyric acid. Yield 98%

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 2.52 (m, 2H),2.67 (t, 2H).

2. 101 ml of oxalyl chloride and 0.1 ml of dimethylformamide was addedto a solution of thus obtained 131 g of the 4,4,4-trifluorobutyric acidin 1 liter of pentane, and the resultant solution was refluxed for threehours. Then the reaction solution was distilled to yield 112 g of4,4,4-trifluorobutyryl chloride in a yield of 76%. (b.p. 103° C./760mmHg)

3. 0.1 ml of carbon tetrachloride was added to a mixture of 20.35 g ofmagnesium(turnings) and 148 ml of ethanol and then heated at 55° C. Amixed solution of 197 ml of ethanol, 700 ml of diethyl ether and 168 gof diethyl malonate was added to the reaction mixture over 1 hour. Twohours later the reaction solution was cooled to -5° C. and 112 g of4,4,4-trifluorobutyryl chloride was added to the solution under anatmosphere of nitrogen, then the resultant reaction mixture was left atan ambient temperature for 1 hour. Then the mixture was allowed to reactfurther 12 hours. After completion of the reaction, the reactionsolution was poured into a 5% hydrochloric acid solution and extractedthree times with diethyl ether. The ether layers were combined andwashed twice with brine and dried over anhydrous magnesium sulfate. Thefiltered ether solution was evaporated under reduced pressure. Theobtained residue was distilled under reduced pressure to yield 179 g ofthe desired 4,4,4-trifluorobutyrylmalonic acid diethyl ester in a yieldof 90%. (b.p. 125°-134° C., 15 mmHg)

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.32 (t, 3H),2.50 (m, 2H), 2.95 (t, 2H), 4.29 (q, 2H), 4.50 (s, 1H).

4. A mixture of 179 g of the 4,4,4-trifluorobutyrylmalonic acid ditheylester thus obtained, 260 ml of water and 322 mg of p-toluenesulfonicacid was refluxed with vigorous stirring for 6 hours. The reactionsolution was then poured into saturated aqueous sodium hydrogencarbonatesolution and extracted three times with diethyl ether. The ether layerswere combined and the combined layer was washed with brine, dried overanhydrous magnesium sulfate. After the drying agent was removed, thesolvent was removed under reduced pressure. The obtained residue wasdistilled inder reduced pressure to yield 98.8 g of the desired ethyl4,4,4-trifluorobutyrylacetate in a yield of 74%. (b.p. 93°-97° C., 15mmHg)

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 1.28 (t, 3H),2.45 (m, 2H), 2.96 (t, 2H), 3.48 (s, 1H), 4.22 (q, 2H).

5. 98.8 g of the ethyl 4,4,4-trifluorobutyrylacetate thus obtained wasadded to 250 ml of a 10% sodium hydroxide solution and vigorouslystirred for 12 hours. The pH value of the reaction solution was brought7.5 with a 10% aqueous sulfuric acid solution. Then 250 ml of toluene,2.86 g of sodium hydrogencarbonate and 6.43 g of hydrosulfite were addedto the solution under an atmosphere of nitrogen and warmed to 37° C. 90g of methyl glyoxal was added over 1 hour and allowed to react for 12hours. After 50 g of sodium chloride was added to the solution, themixture was extracted three times with ethyl acetate. The ethyl acetatelayers were combined and dried over anhydrous magnesium sulfate. Afterremoval of the drying agent, the solvent was removed under reducedpressure. The obtained residue was mixed with 450 ml of 5% sodiumhydroxide solution and vigorously stirred under ice-water cooling. ThepH of the solution was adjusted to 7.3 with a 10% hydrochloric acidsolution and then extracted three times with ethyl acetate. The ethylacetate layer was combined and dried over anhydrous magnesium sulfate.After removal of the drying agent, the solvent was removed under reducedpressure. The obtained residue was distilled under reduced pressure toafford 45 g of the desired(RS)-2-methyl-3-(2,2,2-trifluoroethyl)-4-oxocyclopent-2-en-1-ol in ayield of 50%. (b.p. 100°-133° C., 0.52 mmHg)

¹ H-NMR (CDCl₃, internal standard TMS) δ values (ppm): 2.19 (s, 3H),2.35 (dd, 1H), 2.85 (dd, 1H), 3.08 (q, 2H), 4.82 (brd, 1H).

¹⁹ F-NMR (CDCl₃, internal standard CCl₃ F) δ values (ppm): -65.1(t, 3F).

Formulation examples are described below, parts represent parts byweight.

Formulation example 1 Emulsifiable concentrates

Twenty parts of each of the compounds 1 to 90 are dissolved in 65 partsof xylene, mixed with 15 parts of an emulsifier Solpol 3005X (registeredtrade mark by Toho Chemical), and stirred sufficiently to give 20%emulsifiable concentrates for each compound.

Formulation example 2 Wettable powders

Forty parts of each of the compounds 1 to 90 are mixed first with 5parts of Solpol 3005X and then with 32 parts of Carprex #80 (synthetichydrated silicon hydroxide fine powder: registered trade mark byShionogi & Co. Ltd.) and 23 parts of 300-mesh diatomaceous earth, andstirred with a blender to give 40% wettable powders for each compound.

Formulation example 3 Granules

1.5% granules for each of compounds 1 to 90 are obtained by sufficientlymixing 1.5 parts of each of the compounds and 98.5 parts of AGSORBLVM-MS24/48 (granular carrier of calcined montmorillonite having the particlediameter of 24 to 48 meshes by OIL DRI Corp.) with each other.

Formulation example 4 Microcapsules

A mixture of 10 parts of each of the compounds 1 to 90, 10 parts ofphenylxylylethane, and 0.5 part of 5 Sumijul L-75 (tolylene diisocyanateby Sumitomo Bayer Urethane Ltd.) is added to 20 parts of a 10% aqueoussolution of gum arabic, and stirred with a homomixer to give an emulsionhaving the mean particle diameter of 20 μm. The emulsion is furthermixed with two parts of ethylene glycol and allowed to react in a warmbath of 60° C. for 24 hours to give a microcapsule slurry.

A thickening agent is prepared by dispersing 0.2 parts of xanthan gumand 1.0 part of Veegum R (aluminum magnesium silicate by Sanyo Chemical)in 56.3 parts of ion-exchanged water.

10% microcapsules are obtained by mixing 42.5 parts of the microcapsuleslurry and 57.5 parts of the thickening agent for each of the compounds.

Formulation example 5 Flowables (Water emulsion)

Each of the mixtures of 10 parts of each of the compounds 1 to 90 and 10parts of phenylxylylethane is added to 20 parts of a 10% aqueoussolution of polyethylene glycol, and stirred with a homomixer to give anemulsion having the mean particle diameter of 3 μm.

A thickening agent is obtained by dispersing 0.2 part of xanthan gum and1.0 part of Veegum R (aluminum magnesium silicate by Sanyo Chemical) in58.8 parts of ion-exchanged water. 10% water emulsion is obtained bymixing 40 parts of the emulsion and 60 parts of the thickening agent foreach of the compounds.

Formulation example 6 Dusts

Five parts of each of the compounds 1 to 90 are mixed with 3 parts ofCarprex #80, 0.3 part of PAP, and 91.7 part of 300-mesh talc and stirredwith a blender to give 5% dusts for each of the compounds.

Formulation example 7 Oil solutions

0.1% oil solutions are obtained by dissolving 0.1 part of each of thecompounds 1 to 90 in 5 parts of dichloromethane and mixing the solutionwith 94.9 parts of deodorized kerosine for each of the compounds.

Formulation example 8 Oil-based aerosols

One part of each of the compounds 1 to 90 is mixed dissolved in 5 partsof dichloromethane and 34 parts of deodorized kerosine. Oil-basedaerosol is obtained for each of the compounds by filling an aerosolvessel with the mixture and charging 60 parts of a propellant (liquefiedpetroleum gas) through a valve into the aerosol vessel under pressure.

Formulation example 9 Water-based aerosols

An aerosol vessel is filled with 50 parts of pure water and a mixture of0.6 parts of each of the compounds 1 to 90, 5 parts of xylene, 3.4 partsof deodorized kerosine, and 1 part of an emulsifier Atmos 300(registered trade mark by Atlas Chemical). Water-based aerosol isobtained for each of the compounds by charging 40 parts of a propellant(liquefied petroleum gas) through a valve into the aerosol vessel underthe applied pressure.

Formulation example 10 Mosquito-coils

A solution prepared by dissolving 0.3 g of each of the compounds 1 to 90in each 20 ml of acetone is homogeneously mixed with 99.7 g of a carrierfor a mosquito-coil (mixture of powder of Machilus thunbergii Sieb. etZucc., lees powder and wood powder at the ratio of 4:3:3). After 120 mlof water is added, the mixture is kneaded sufficiently, molded, anddried to give mosquito-coil for each of the compounds.

Formulation example 11 Mosquito-mats for electric heating fumigation

A total 10 ml of a solution is prepared by dissolving 0.8 g of each ofthe compounds 1 to 90 and 0.4 g of piperonyl butoxide in acetone. Eachmosquito-mat for electric heating fumigation is obtained by impregnatinga base material (a plate of compacted fibrils of a mixture of pulp andcotton linters: 2.5 cm×1.5 cm×0.3 cm) homogeneously with 0.5 ml of thesolution.

Formulation example 12 Solutions for electric heating fumigation

Heating fumigation comprising dipping a part of porous absorptive wick,which is prepared by calcinating a caking of a powdery inorganicsubstance with a binding agent, in a solution of 3 parts of each of thecompounds 1 to 90 in 97 parts of deoderized kerosine contained in avessel of vinyl chloride and indirectly heating the wick around the topto fumigate the compound.

Formulation example 13 Fumigants

Fumigant is prepared for each of the compounds 1 to 90 by impregnating aporous ceramic plate (4.0 cm×4.0 cm×1.2 cm) with a solution prepared bydissolving 100 mg of each of the compounds 1 to 90 in an appropriateamount of acetone.

Formulation example 14 Volatile agents

Volatile agent is prepared for each of the compounds 1 to 90 by applyinga solution, prepared by dissolving 100 mg of each of the compounds in anappropriate amount of acetone, onto filter paper (2 cm×2 cm×0.3 mm) andevaporating the acetone.

Formulation example 15 Mite-repellent sheets

Mite-repellent sheet is prepared by impregnating filter paper with anacetone solution containing each of the compounds 1 to 90 so that theconcentration of each of the compounds is 1 g/1 m² and evaporating theacetone.

The compounds of the present invention were respectively tested as anactive ingredient of an insecticide, an acaricide, or a soil insectpest. In the description below, the compounds are shown by the numbersin Tables 1 whereas compounds used as controls ((RS)-isomer on thealcohol site and dl-cis, trans isomer on the acid site) are shown by thesymbols in Table 2.

                                      TABLE 2                                     __________________________________________________________________________    Symbols                                                                       for                                                                           chemical                                                                           Chemical                                                                 compound                                                                           Structure              Remarks                                           __________________________________________________________________________          ##STR143##            A compound disclosed in Japanese Patent Kokai                                 (Laying Open) S-56-75459 as a compound 1-A        B                                                                                   ##STR144##            A compound disclosed in Japanese Patent Kokai                                 (Laying Open) S-57-67537 as a compound (1)        C                                                                                   ##STR145##            Allethrin commercial insecticide                  __________________________________________________________________________

Biological test 1

Each compound was formulated into an emulsifiable concentrates accordingto Formulation example 1. Five milliliters of the emulsifiableconcentrates previously diluted with water were mixed with 50 g ofsterilized soil (16 mesh) so that the concentration of the activeingredient in soil was 10 ppm. The soil was placed in a polyethylene cup(diameter: 5.6 cm, depth: 5.8 cm), and two corn grains germinated tohave the root of approximately 2 cm were planted in the soil. Ten3-instar larvae of Diabrotica undecimpunctata howardi Barber were lefton the soil. After three days, the mortality of the larvae and thedamage of the grains were observed. The damage was evaluated accordingto the following criteria:

    ______________________________________                                        Damage        Criteria                                                        ______________________________________                                        ++            equivalent damage to non-treated                                              soil                                                            +             heavy damage                                                    +-            slight damage                                                   -             no damage                                                       ______________________________________                                    

Table 3 shows the mortality of the larvae (%) and evaluation of thedamage.

                  TABLE 3                                                         ______________________________________                                        Compound       Mortality (%)                                                                            Damage                                              ______________________________________                                        1              100        --                                                  4              100        --                                                  5              100        --                                                  9              100        --                                                  11             100        --                                                  12             100        --                                                  15             100        --                                                  20             100        --                                                  21             100        --                                                  27             100        --                                                  43             100        --                                                  44             100        --                                                  54             100        --                                                  ______________________________________                                    

Biological test 2

The present compound was diluted with acetone, applied homogeneouslyonto a bottom of an aluminum plate (inner diameter: 10 cm; depth: 3 cm;bottom area: 78.5 cm²) at the concentration of 100 mg/m², and air-dried.Ten cockroaches (Blattella germanica) including five males and fivefemales were left on and forcibly brought into contact with the treatedface of the aluminum plate. After two hours, the rate of knocked-downinsects was examined, and the results are shown in Table 4.

                  TABLE 4                                                         ______________________________________                                                    Rate of                                                           Compound    knocked-down insects (%)                                          ______________________________________                                        1           100                                                               5           100                                                               6           100                                                               8           100                                                               9           100                                                               10          100                                                               11          100                                                               12          100                                                               14          100                                                               17          100                                                               19          100                                                               20          100                                                               21          100                                                               27          100                                                               29          100                                                               32          100                                                               37          100                                                               44          100                                                               54          100                                                               ______________________________________                                    

Biological test 3

Ten cockroaches (Blattella germanica) including five males and fivefemales were left in a polyethylene cup (diameter: 9 cm) of which wallsurface was thinly applied with vaseline. The cup was sealed with a16-mesh nylon net and placed in a glass cylinder (inner diameter: 10 cm;depth: 37 cm). 0.1% (w/w) oil solution prepared from the presentcompounds according to Formulation example 7 was sprayed from an upperend of the cylinder with a spray gun at 0.6 atmospheric pressure. Aftertwenty minutes, the insects were taken out and placed in anotherpolyethylene cup with filter paper laid inside thereof. The insects weregiven water. After three days, the mortality of the insects wasexamined, and the results are shown in Table 5.

                  TABLE 5                                                         ______________________________________                                        Compound         Mortality (%)                                                ______________________________________                                        1                100                                                          2                100                                                          5                100                                                          6                100                                                          9                100                                                          12               100                                                          14               100                                                          17               100                                                          20               100                                                          21               100                                                          22               100                                                          24               100                                                          29               100                                                          37               100                                                          Oil solution containing                                                                        0                                                            no active ingredient                                                          ______________________________________                                    

Biological test 4

Mosquito-coil containing the present compound in an amount of 0.3% (w/w)was prepared according to Formulation example 10 for the presentcompounds. Ten female mosquitoes (Culex pipiens pallens) were left in aglass chamber (70cm×70 cm×70 cm: 0.34 m³) and 1.0 g of the mosquito-coilhaving both ends lit was placed in the glass chamber. After 24 minutes,the rate of knocked-down insects was examined, and the results are shownin Table 6.

                  TABLE 6                                                         ______________________________________                                                     Rate of knocked-down                                             Compound     insects (%)                                                      ______________________________________                                        1            100                                                              2            100                                                              5            100                                                              6            100                                                              8            100                                                              9            100                                                              10           100                                                              11           100                                                              12           100                                                              15           100                                                              17           100                                                              19           100                                                              20           100                                                              21           100                                                              22           100                                                              24           100                                                              27           100                                                              29           100                                                              32           100                                                              37           100                                                              43           100                                                              44           100                                                              54           100                                                              72           100                                                              ______________________________________                                    

Biological test 5

After 0.64 ml of a 0.05% (w/v) acetone solution of the present compoundswas dropped into an aluminum plate (bottom diameter: 7 cm), acetone wasair-dried. Twenty female house flies (Musca domestica) were left in apolyethylene cup (diameter: 9 cm; depth: 4.5 cm), and the cup was sealedwith a 16-mesh nylon net to prevent direct contact of the flies with thecompound. The cup was placed upside down on the aluminum plate at 25° C.for 120 minutes. The cup was then removed from the aluminum plate, andwater and feed were given to the flies. After twenty-four hours, themortality was examined (two replicate), and the results are shown inTable 7.

                  TABLE 7                                                         ______________________________________                                        Compound      Mortality (%)                                                   ______________________________________                                        1             100                                                             2             100                                                             6             100                                                             8             100                                                             9             100                                                             10            100                                                             11            100                                                             12            100                                                             15            100                                                             17            100                                                             19            100                                                             21            100                                                             22            100                                                             27            100                                                             34            100                                                             43            100                                                             54            100                                                             A             0                                                               B             0                                                               C             0                                                               ______________________________________                                    

Biological test 6

Volatile agent prepared according to Formulation example 14 wassuspended inner space of a polyethylene cup 1 (bottom diameter: 10 cm,diameter of opening: 12.5 cm; depth 9.5 cm; volume 950 cm³) placedupside down. Ten 21-28 day-instar larvae of Tineola bisselliella wereleft in another polyethylene cup 2 having the same size as the cup 1 andcontaining wool muslin cloth (2 cm×2 cm: approximately 100 mg) thereinlaid on the bottom thereof. The cups 1 and 2 were joined together andsealed at their openings, and left at 25° C. for one week. The cups werethen opened, and the mortality of moths was examined. Table 8 shows theresults.

                  TABLE 8                                                         ______________________________________                                        Compound      Mortality (%)                                                   ______________________________________                                        1             100                                                             2             100                                                             6             100                                                             8             100                                                             9             100                                                             10            100                                                             11            100                                                             12            100                                                             14            100                                                             15            100                                                             17            100                                                             19            100                                                             20            100                                                             21            100                                                             22            100                                                             24            100                                                             27            100                                                             29            100                                                             32            100                                                             34            100                                                             37            100                                                             43            100                                                             45            100                                                             54            100                                                             A             0                                                               B             0                                                               C             0                                                               ______________________________________                                    

Biological test 7

Mite-repellent sheet prepared according to Formulation example 15 wascut into a circle of 4 cm in diameter. Approximately fifty mites(Dermatophagoides farinae) were left on the surface of the sheet. Afterone day, the number of mites, which were dead or trapped by an adhesivesubstance applied on the circumference of the sheet for preventingescape, was counted. The efficacy was evaluated by the ratio of thenumber of the dead or trapped mites to the total number of mites used.The results are shown in Table 9.

                  TABLE 9                                                         ______________________________________                                        Compound      Efficacy (%)                                                    ______________________________________                                        1             100                                                             2             100                                                             4             100                                                             5             100                                                             6             100                                                             11            100                                                             12            100                                                             15            100                                                             17            100                                                             21            100                                                             22            100                                                             29            100                                                             32            100                                                             34            100                                                             43            100                                                             54            100                                                             no treatment  8                                                               ______________________________________                                    

What is claimed is:
 1. A compound represented by the formula: ##STR146##wherein R₁ represents a hydrogen atom or a methyl group; R₂ represents a1-methyl-2-propenyl group, a 1-methyl-2-propynyl group, a3,3-dihalogeno-1-methyl-2-propenyl group or a C₁ -C₆ alkyl group whichmay be substituted with at least one halogen atom; and A' represents ahydrogen atom or a protecting group for a hydroxyl group.
 2. A compoundaccording to claim 1, wherein A' represents H, and said compound is analcohol.
 3. A compound according to claim 2, wherein R₂ represents an C₁-C₆ alkyl group which may be substituted with at least one halogen atom.4. A compound according to claim 3, wherein R₂ is an ethyl group, a2-fluoroethyl group, a 3-fluoropropyl group or a 2,2,2-trifluoroethylgroup.
 5. A compound according to claim 1, wherein said compound is analcohol derivative in which A' represents a protecting group for ahydroxyl group.
 6. A compound according to claim 5, wherein A'represents a (C₁ -C₂)alkyl group substituted with (C₁ -C₂)alkoxy groupat the α-position, a tri(C₁ -C₆)alkylsilyl group, 2-tetrahydrofuranylgroup or 2-tetrahydropyranyl group.